Canonical Allele Identifier: CA617605772

Gene: CAPN3

Linked Data

• dbSNP Id: rs1456822412
• gnomAD v2: 15-42686357-A-C
• gnomAD v3: 15-42394159-A-C
• gnomAD v4: 15-42394159-A-C
• MyVariant Identifiers: chr15:g.42686357A>C (hg19) ; chr15:g.42394159A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42394159A>C , CM000677.2:g.42394159A>C	GRCh38
NC_000015.9:g.42686357A>C , CM000677.1:g.42686357A>C	GRCh37
NC_000015.8:g.40473649A>C	NCBI36
NG_008660.1:g.51057A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.886-97A>C	ENSP00000183936.4:n.886-97A>C
ENST00000357568.8:c.1030-97A>C	ENSP00000350181.3:n.1030-97A>C
ENST00000397163.8:c.1030-97A>C MANE Select	ENSP00000380349.3:n.1030-97A>C
ENST00000466369.5:n.1539-97A>C
ENST00000483208.5:n.1261-97A>C
ENST00000495723.1:n.1261-97A>C
ENST00000549793.5:n.1261-97A>C
ENST00000638141.2:n.901-97A>C
ENST00000673658.1:n.14-97A>C
ENST00000673705.1:c.71-2641A>C	ENSP00000501021.1:n.71-2641A>C
ENST00000318023.11:c.886-97A>C	ENSP00000326281.8:n.886-97A>C
ENST00000349748.7:c.886-97A>C	ENSP00000183936.4:n.886-97A>C
ENST00000357568.7:c.1030-97A>C	ENSP00000350181.3:n.1030-97A>C
ENST00000397163.7:c.1030-97A>C	ENSP00000380349.3:n.1030-97A>C
NM_000070.2:c.1030-97A>C	NP_000061.1:n.1030-97A>C
NM_024344.1:c.1030-97A>C	NP_077320.1:n.1030-97A>C
NM_173087.1:c.886-97A>C	NP_775110.1:n.886-97A>C
NM_000070.3:c.1030-97A>C MANE Select	NP_000061.1:n.1030-97A>C
NM_024344.2:c.1030-97A>C	NP_077320.1:n.1030-97A>C
NM_173087.2:c.886-97A>C	NP_775110.1:n.886-97A>C