Canonical Allele Identifier: CA2628030836

Gene: CAPN3

Linked Data

• gnomAD v4: 15-42392517-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42392517A>T , CM000677.2:g.42392517A>T	GRCh38
NC_000015.9:g.42684715A>T , CM000677.1:g.42684715A>T	GRCh37
NC_000015.8:g.40472007A>T	NCBI36
NG_008660.1:g.49415A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000349748.8:c.802-122A>T	ENSP00000183936.4:n.802-122A>T
ENST00000357568.8:c.946-122A>T	ENSP00000350181.3:n.946-122A>T
ENST00000397163.8:c.946-122A>T MANE Select	ENSP00000380349.3:n.946-122A>T
ENST00000466369.5:n.1455-122A>T
ENST00000483208.5:n.1177-122A>T
ENST00000495723.1:n.1177-122A>T
ENST00000549793.5:n.1177-122A>T
ENST00000638141.2:n.817-122A>T
ENST00000673705.1:c.71-4283A>T	ENSP00000501021.1:n.71-4283A>T
ENST00000318023.11:c.802-122A>T	ENSP00000326281.8:n.802-122A>T
ENST00000349748.7:c.802-122A>T	ENSP00000183936.4:n.802-122A>T
ENST00000357568.7:c.946-122A>T	ENSP00000350181.3:n.946-122A>T
ENST00000397163.7:c.946-122A>T	ENSP00000380349.3:n.946-122A>T
NM_000070.2:c.946-122A>T	NP_000061.1:n.946-122A>T
NM_024344.1:c.946-122A>T	NP_077320.1:n.946-122A>T
NM_173087.1:c.802-122A>T	NP_775110.1:n.802-122A>T
NM_000070.3:c.946-122A>T MANE Select	NP_000061.1:n.946-122A>T
NM_024344.2:c.946-122A>T	NP_077320.1:n.946-122A>T
NM_173087.2:c.802-122A>T	NP_775110.1:n.802-122A>T