Canonical Allele Identifier: CA7510862

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 549977
• ClinVar RCV Id: RCV000664576
• dbSNP Id: rs767281996
• ExAC: 15:42652146 G / A
• gnomAD v2: 15-42652146-G-A
• gnomAD v3: 15-42359948-G-A
• gnomAD v4: 15-42359948-G-A
• MyVariant Identifiers: chr15:g.42652146G>A (hg19) ; chr15:g.42359948G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42359948G>A , CM000677.2:g.42359948G>A	GRCh38
NC_000015.9:g.42652146G>A , CM000677.1:g.42652146G>A	GRCh37
NC_000015.8:g.40439438G>A	NCBI36
NG_008660.1:g.16846G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000349748.8:c.143G>A	ENSP00000183936.4:p.Ser48Asn
ENST00000357568.8:c.143G>A	ENSP00000350181.3:p.Ser48Asn
ENST00000397163.8:c.143G>A MANE Select	ENSP00000380349.3:p.Ser48Asn
ENST00000466369.5:n.540+5495G>A
ENST00000483208.5:n.540+5495G>A
ENST00000495723.1:n.540+5495G>A
ENST00000549793.5:n.540+5495G>A
ENST00000318023.11:c.143G>A	ENSP00000326281.8:p.Ser48Asn
ENST00000349748.7:c.143G>A	ENSP00000183936.4:p.Ser48Asn
ENST00000357568.7:c.143G>A	ENSP00000350181.3:p.Ser48Asn
ENST00000397163.7:c.143G>A	ENSP00000380349.3:p.Ser48Asn
NM_000070.2:c.143G>A	NP_000061.1:p.Ser48Asn
NM_024344.1:c.143G>A	NP_077320.1:p.Ser48Asn
NM_173087.1:c.143G>A	NP_775110.1:p.Ser48Asn
NM_000070.3:c.143G>A MANE Select	NP_000061.1:p.Ser48Asn
NM_024344.2:c.143G>A	NP_077320.1:p.Ser48Asn
NM_173087.2:c.143G>A	NP_775110.1:p.Ser48Asn