ClinVar

NM_000070.3(CAPN3):c.2099T>A (p.Met700Lys)

Gene:

CAPN3:calpain 3 [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Cytogenetic location:

15q15.1

Genomic location:

• Chr15: 42409979 (on Assembly GRCh38)
• Chr15: 42702177 (on Assembly GRCh37)

Preferred name:

NM_000070.3(CAPN3):c.2099T>A (p.Met700Lys)

HGVS:

• NC_000015.10:g.42409979T>A
• NG_008660.1:g.66877T>A
• NM_000070.3:c.2099T>AMANE SELECT
• NM_024344.2:c.2081T>A
• NM_173087.2:c.1823T>A
• NM_173088.2:c.563T>A
• NM_173089.2:c.104T>A
• NM_173090.2:c.104T>A
• NM_212464.2:c.*1197T>A
• NM_212467.2:c.*1774T>A
• NP_000061.1:p.Met700Lys
• NP_077320.1:p.Met694Lys
• NP_775110.1:p.Met608Lys
• NP_775111.1:p.Met188Lys
• NP_775112.1:p.Met35Lys
• NP_775113.1:p.Met35Lys
• LRG_849t1:c.2099T>A
• LRG_849:g.66877T>A
• LRG_849p1:p.Met700Lys
• NC_000015.9:g.42702177T>A
• NM_000070.2:c.2099T>A

This HGVS expression did not pass validation

Protein change:

M188K

Molecular consequence:

• NM_000070.3:c.2099T>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_024344.2:c.2081T>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_173087.2:c.1823T>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_173088.2:c.563T>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_173089.2:c.104T>A - missense variant - [Sequence Ontology: SO:0001583]
• NM_173090.2:c.104T>A - missense variant - [Sequence Ontology: SO:0001583]