Canonical Allele Identifier: CA489885112

Gene: CAPN3

Linked Data

• MyVariant Identifiers: chr15:g.42695105T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42402907T>A , CM000677.2:g.42402907T>A	GRCh38
NC_000015.9:g.42695105T>A , CM000677.1:g.42695105T>A	GRCh37
NC_000015.8:g.40482397T>A	NCBI36
NG_008660.1:g.59805T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1506T>A	ENSP00000183936.4:p.Pro502=
ENST00000357568.8:c.1650T>A	ENSP00000350181.3:p.Pro550=
ENST00000397163.8:c.1650T>A MANE Select	ENSP00000380349.3:p.Pro550=
ENST00000466369.5:n.2159T>A
ENST00000483208.5:n.2539T>A
ENST00000495723.1:n.2539T>A
ENST00000549793.5:n.1881T>A
ENST00000638141.2:n.1521T>A
ENST00000673646.1:c.114T>A	ENSP00000501007.1:p.Pro38=
ENST00000673705.1:c.309+3255T>A	ENSP00000501021.1:n.309+3255T>A
ENST00000673813.1:n.572T>A
ENST00000318023.11:c.1506T>A	ENSP00000326281.8:p.Pro502=
ENST00000349748.7:c.1506T>A	ENSP00000183936.4:p.Pro502=
ENST00000357568.7:c.1650T>A	ENSP00000350181.3:p.Pro550=
ENST00000397163.7:c.1650T>A	ENSP00000380349.3:p.Pro550=
ENST00000397200.8:c.114T>A	ENSP00000380384.4:p.Pro38=
ENST00000567071.5:c.109T>A
ENST00000569827.5:c.114T>A	ENSP00000454379.1:p.Pro38=
NM_000070.2:c.1650T>A	NP_000061.1:p.Pro550=
NM_024344.1:c.1650T>A	NP_077320.1:p.Pro550=
NM_173087.1:c.1506T>A	NP_775110.1:p.Pro502=
NM_173088.1:c.114T>A	NP_775111.1:p.Pro38=
NM_000070.3:c.1650T>A MANE Select	NP_000061.1:p.Pro550=
NM_024344.2:c.1650T>A	NP_077320.1:p.Pro550=
NM_173087.2:c.1506T>A	NP_775110.1:p.Pro502=
NM_173088.2:c.114T>A	NP_775111.1:p.Pro38=