Canonical Allele Identifier: CA269844801

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 2914136
• ClinVar RCV Id: RCV003632860
• dbSNP Id: rs933881512
• gnomAD v4: 15-42403011-T-C
• MyVariant Identifiers: chr15:g.42695209T>C (hg19) ; chr15:g.42403011T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42403011T>C , CM000677.2:g.42403011T>C	GRCh38
NC_000015.9:g.42695209T>C , CM000677.1:g.42695209T>C	GRCh37
NC_000015.8:g.40482501T>C	NCBI36
NG_008660.1:g.59909T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1601+9T>C	ENSP00000183936.4:n.1601+9T>C
ENST00000357568.8:c.1745+9T>C	ENSP00000350181.3:n.1745+9T>C
ENST00000397163.8:c.1745+9T>C MANE Select	ENSP00000380349.3:n.1745+9T>C
ENST00000466369.5:n.2254+9T>C
ENST00000483208.5:n.2634+9T>C
ENST00000495723.1:n.2634+9T>C
ENST00000549793.5:n.1976+9T>C
ENST00000638141.2:n.1616+9T>C
ENST00000673646.1:c.209+9T>C	ENSP00000501007.1:n.209+9T>C
ENST00000673705.1:c.309+3359T>C	ENSP00000501021.1:n.309+3359T>C
ENST00000673813.1:n.580+96T>C
ENST00000318023.11:c.1601+9T>C	ENSP00000326281.8:n.1601+9T>C
ENST00000349748.7:c.1601+9T>C	ENSP00000183936.4:n.1601+9T>C
ENST00000357568.7:c.1745+9T>C	ENSP00000350181.3:n.1745+9T>C
ENST00000397163.7:c.1745+9T>C	ENSP00000380349.3:n.1745+9T>C
ENST00000397200.8:c.209+9T>C	ENSP00000380384.4:n.209+9T>C
ENST00000567071.5:c.204+9T>C
ENST00000569827.5:c.209+9T>C	ENSP00000454379.1:n.209+9T>C
NM_000070.2:c.1745+9T>C	NP_000061.1:n.1745+9T>C
NM_024344.1:c.1745+9T>C	NP_077320.1:n.1745+9T>C
NM_173087.1:c.1601+9T>C	NP_775110.1:n.1601+9T>C
NM_173088.1:c.209+9T>C	NP_775111.1:n.209+9T>C
NM_000070.3:c.1745+9T>C MANE Select	NP_000061.1:n.1745+9T>C
NM_024344.2:c.1745+9T>C	NP_077320.1:n.1745+9T>C
NM_173087.2:c.1601+9T>C	NP_775110.1:n.1601+9T>C
NM_173088.2:c.209+9T>C	NP_775111.1:n.209+9T>C