Canonical Allele Identifier: CA392000325

Gene: CAPN3

Linked Data

• MyVariant Identifiers: chr15:g.42695110G>C (hg19) ; chr15:g.42402912G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42402912G>C , CM000677.2:g.42402912G>C	GRCh38
NC_000015.9:g.42695110G>C , CM000677.1:g.42695110G>C	GRCh37
NC_000015.8:g.40482402G>C	NCBI36
NG_008660.1:g.59810G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1511G>C	ENSP00000183936.4:p.Ser504Thr
ENST00000357568.8:c.1655G>C	ENSP00000350181.3:p.Ser552Thr
ENST00000397163.8:c.1655G>C MANE Select	ENSP00000380349.3:p.Ser552Thr
ENST00000466369.5:n.2164G>C
ENST00000483208.5:n.2544G>C
ENST00000495723.1:n.2544G>C
ENST00000549793.5:n.1886G>C
ENST00000638141.2:n.1526G>C
ENST00000673646.1:c.119G>C	ENSP00000501007.1:p.Ser40Thr
ENST00000673705.1:c.309+3260G>C	ENSP00000501021.1:n.309+3260G>C
ENST00000673813.1:n.577G>C
ENST00000318023.11:c.1511G>C	ENSP00000326281.8:p.Ser504Thr
ENST00000349748.7:c.1511G>C	ENSP00000183936.4:p.Ser504Thr
ENST00000357568.7:c.1655G>C	ENSP00000350181.3:p.Ser552Thr
ENST00000397163.7:c.1655G>C	ENSP00000380349.3:p.Ser552Thr
ENST00000397200.8:c.119G>C	ENSP00000380384.4:p.Ser40Thr
ENST00000567071.5:c.114G>C
ENST00000569827.5:c.119G>C	ENSP00000454379.1:p.Ser40Thr
NM_000070.2:c.1655G>C	NP_000061.1:p.Ser552Thr
NM_024344.1:c.1655G>C	NP_077320.1:p.Ser552Thr
NM_173087.1:c.1511G>C	NP_775110.1:p.Ser504Thr
NM_173088.1:c.119G>C	NP_775111.1:p.Ser40Thr
NM_000070.3:c.1655G>C MANE Select	NP_000061.1:p.Ser552Thr
NM_024344.2:c.1655G>C	NP_077320.1:p.Ser552Thr
NM_173087.2:c.1511G>C	NP_775110.1:p.Ser504Thr
NM_173088.2:c.119G>C	NP_775111.1:p.Ser40Thr