Canonical Allele Identifier: CA2628031103

Gene: CAPN3

Linked Data

• gnomAD v4: 15-42394215-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42394215G>T , CM000677.2:g.42394215G>T	GRCh38
NC_000015.9:g.42686413G>T , CM000677.1:g.42686413G>T	GRCh37
NC_000015.8:g.40473705G>T	NCBI36
NG_008660.1:g.51113G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000349748.8:c.886-41G>T	ENSP00000183936.4:n.886-41G>T
ENST00000357568.8:c.1030-41G>T	ENSP00000350181.3:n.1030-41G>T
ENST00000397163.8:c.1030-41G>T MANE Select	ENSP00000380349.3:n.1030-41G>T
ENST00000466369.5:n.1539-41G>T
ENST00000483208.5:n.1261-41G>T
ENST00000495723.1:n.1261-41G>T
ENST00000549793.5:n.1261-41G>T
ENST00000638141.2:n.901-41G>T
ENST00000673658.1:n.14-41G>T
ENST00000673705.1:c.71-2585G>T	ENSP00000501021.1:n.71-2585G>T
ENST00000318023.11:c.886-41G>T	ENSP00000326281.8:n.886-41G>T
ENST00000349748.7:c.886-41G>T	ENSP00000183936.4:n.886-41G>T
ENST00000357568.7:c.1030-41G>T	ENSP00000350181.3:n.1030-41G>T
ENST00000397163.7:c.1030-41G>T	ENSP00000380349.3:n.1030-41G>T
NM_000070.2:c.1030-41G>T	NP_000061.1:n.1030-41G>T
NM_024344.1:c.1030-41G>T	NP_077320.1:n.1030-41G>T
NM_173087.1:c.886-41G>T	NP_775110.1:n.886-41G>T
NM_000070.3:c.1030-41G>T MANE Select	NP_000061.1:n.1030-41G>T
NM_024344.2:c.1030-41G>T	NP_077320.1:n.1030-41G>T
NM_173087.2:c.886-41G>T	NP_775110.1:n.886-41G>T