Canonical Allele Identifier: CA618001556

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 1088268
• ClinVar RCV Id: RCV001406678
• dbSNP Id: rs1278180136
• gnomAD v2: 15-42695208-C-G
• gnomAD v3: 15-42403010-C-G
• gnomAD v4: 15-42403010-C-G
• MyVariant Identifiers: chr15:g.42695208C>G (hg19) ; chr15:g.42403010C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42403010C>G , CM000677.2:g.42403010C>G	GRCh38
NC_000015.9:g.42695208C>G , CM000677.1:g.42695208C>G	GRCh37
NC_000015.8:g.40482500C>G	NCBI36
NG_008660.1:g.59908C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1601+8C>G	ENSP00000183936.4:n.1601+8C>G
ENST00000357568.8:c.1745+8C>G	ENSP00000350181.3:n.1745+8C>G
ENST00000397163.8:c.1745+8C>G MANE Select	ENSP00000380349.3:n.1745+8C>G
ENST00000466369.5:n.2254+8C>G
ENST00000483208.5:n.2634+8C>G
ENST00000495723.1:n.2634+8C>G
ENST00000549793.5:n.1976+8C>G
ENST00000638141.2:n.1616+8C>G
ENST00000673646.1:c.209+8C>G	ENSP00000501007.1:n.209+8C>G
ENST00000673705.1:c.309+3358C>G	ENSP00000501021.1:n.309+3358C>G
ENST00000673813.1:n.580+95C>G
ENST00000318023.11:c.1601+8C>G	ENSP00000326281.8:n.1601+8C>G
ENST00000349748.7:c.1601+8C>G	ENSP00000183936.4:n.1601+8C>G
ENST00000357568.7:c.1745+8C>G	ENSP00000350181.3:n.1745+8C>G
ENST00000397163.7:c.1745+8C>G	ENSP00000380349.3:n.1745+8C>G
ENST00000397200.8:c.209+8C>G	ENSP00000380384.4:n.209+8C>G
ENST00000567071.5:c.204+8C>G
ENST00000569827.5:c.209+8C>G	ENSP00000454379.1:n.209+8C>G
NM_000070.2:c.1745+8C>G	NP_000061.1:n.1745+8C>G
NM_024344.1:c.1745+8C>G	NP_077320.1:n.1745+8C>G
NM_173087.1:c.1601+8C>G	NP_775110.1:n.1601+8C>G
NM_173088.1:c.209+8C>G	NP_775111.1:n.209+8C>G
NM_000070.3:c.1745+8C>G MANE Select	NP_000061.1:n.1745+8C>G
NM_024344.2:c.1745+8C>G	NP_077320.1:n.1745+8C>G
NM_173087.2:c.1601+8C>G	NP_775110.1:n.1601+8C>G
NM_173088.2:c.209+8C>G	NP_775111.1:n.209+8C>G