Canonical Allele Identifier: CA14198265

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 678271
• ClinVar RCV Id: RCV000837850
• dbSNP Id: rs28364416
• gnomAD v2: 15-42680910-C-T
• gnomAD v3: 15-42388712-C-T
• gnomAD v4: 15-42388712-C-T
• MyVariant Identifiers: chr15:g.42680910C>T (hg19) ; chr15:g.42388712C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42388712C>T , CM000677.2:g.42388712C>T	GRCh38
NC_000015.9:g.42680910C>T , CM000677.1:g.42680910C>T	GRCh37
NC_000015.8:g.40468202C>T	NCBI36
NG_008660.1:g.45610C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.633-216C>T	ENSP00000183936.4:n.633-216C>T
ENST00000357568.8:c.633-216C>T	ENSP00000350181.3:n.633-216C>T
ENST00000397163.8:c.633-216C>T MANE Select	ENSP00000380349.3:n.633-216C>T
ENST00000466369.5:n.1142-216C>T
ENST00000483208.5:n.864-216C>T
ENST00000495723.1:n.864-216C>T
ENST00000549793.5:n.864-216C>T
ENST00000638141.2:n.648-216C>T
ENST00000673705.1:c.70+4160C>T	ENSP00000501021.1:n.70+4160C>T
ENST00000318023.11:c.633-216C>T	ENSP00000326281.8:n.633-216C>T
ENST00000349748.7:c.633-216C>T	ENSP00000183936.4:n.633-216C>T
ENST00000357568.7:c.633-216C>T	ENSP00000350181.3:n.633-216C>T
ENST00000397163.7:c.633-216C>T	ENSP00000380349.3:n.633-216C>T
NM_000070.2:c.633-216C>T	NP_000061.1:n.633-216C>T
NM_024344.1:c.633-216C>T	NP_077320.1:n.633-216C>T
NM_173087.1:c.633-216C>T	NP_775110.1:n.633-216C>T
NM_000070.3:c.633-216C>T MANE Select	NP_000061.1:n.633-216C>T
NM_024344.2:c.633-216C>T	NP_077320.1:n.633-216C>T
NM_173087.2:c.633-216C>T	NP_775110.1:n.633-216C>T