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These reference sequences exist independently of genome builds. Explain
These reference sequences are curated independently of the genome
annotation cycle, so their versions may not match the RefSeq versions in the current
genome build. Identify version mismatches by comparing the version of the RefSeq in
this section to the one reported in Genomic regions,
transcripts, and products above.
mRNA and Protein(s)
-
NM_001008784.4 → NP_001008784.2 cell surface glycoprotein CD200 receptor 2 isoform 1 precursor
See identical proteins and their annotated locations for NP_001008784.2
Status: VALIDATED
- Description
- Transcript Variant: This variant (1, coding) represents the allele encoded by the GRCh38 reference genome and encodes isoform (1).
- Source sequence(s)
-
AC074044, AC092892
- Consensus CDS
-
CCDS43131.1
- UniProtKB/Swiss-Prot
- Q6Q8B3, Q6WHB7
- Related
- ENSP00000381272.1, ENST00000398214.5
- Conserved Domains (1) summary
-
- cl11960
Location:156 → 224
- Ig; Immunoglobulin domain
-
NM_001199215.3 → NP_001186144.1 cell surface glycoprotein CD200 receptor 2 isoform 2
See identical proteins and their annotated locations for NP_001186144.1
Status: VALIDATED
- Description
- Transcript Variant: This variant (2, coding) represents the allele encoded by the GRCh38 reference genome and encodes isoform (2).
- Source sequence(s)
-
AC074044, AC092892
- Consensus CDS
-
CCDS56267.1
- Related
- ENSP00000418413.1, ENST00000488794.6
- Conserved Domains (1) summary
-
- cl11960
Location:135 → 203
- Ig; Immunoglobulin domain
-
NM_001370552.3 → NP_001357481.1 cell surface glycoprotein CD200 receptor 2 isoform 2
Status: VALIDATED
- Description
- Transcript Variant: This variant (3, coding) represents the allele encoded by the GRCh38 reference genome and encodes isoform (2).
- Source sequence(s)
-
AC074044, AC092892
- Consensus CDS
-
CCDS56267.1
- Conserved Domains (1) summary
-
- cl11960
Location:135 → 203
- Ig; Immunoglobulin domain
RNA
-
NR_178042.1 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (1, non-coding) uses the same exon combination as variant (1, coding) but represents the allele present on the T2T-CHM13v2.0 genome assembly. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
CP068275
-
NR_178043.1 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (2, non-coding) uses the same exon combination as variant (2, coding) but represents the allele present on the T2T-CHM13v2.0 genome assembly. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
CP068275
-
NR_178044.1 RNA Sequence
Status: VALIDATED
- Description
- Transcript Variant: This variant (3, non-coding) uses the same exon combination as variant (3, coding) but represents the allele present on the T2T-CHM13v2.0 genome assembly. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
- Source sequence(s)
-
CP068275
The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference GRCh38.p14 Primary Assembly
Genomic
-
NC_000003.12 Reference GRCh38.p14 Primary Assembly
- Range
-
112815711..112846864 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060927.1 Alternate T2T-CHM13v2.0
- Range
-
115536646..115567808 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)