Canonical Allele Identifier: CA392000317

Gene: CAPN3

Linked Data

• dbSNP Id: rs2141203114
• MyVariant Identifiers: chr15:g.42695106C>A (hg19) ; chr15:g.42402908C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42402908C>A , CM000677.2:g.42402908C>A	GRCh38
NC_000015.9:g.42695106C>A , CM000677.1:g.42695106C>A	GRCh37
NC_000015.8:g.40482398C>A	NCBI36
NG_008660.1:g.59806C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1507C>A	ENSP00000183936.4:p.Pro503Thr
ENST00000357568.8:c.1651C>A	ENSP00000350181.3:p.Pro551Thr
ENST00000397163.8:c.1651C>A MANE Select	ENSP00000380349.3:p.Pro551Thr
ENST00000466369.5:n.2160C>A
ENST00000483208.5:n.2540C>A
ENST00000495723.1:n.2540C>A
ENST00000549793.5:n.1882C>A
ENST00000638141.2:n.1522C>A
ENST00000673646.1:c.115C>A	ENSP00000501007.1:p.Pro39Thr
ENST00000673705.1:c.309+3256C>A	ENSP00000501021.1:n.309+3256C>A
ENST00000673813.1:n.573C>A
ENST00000318023.11:c.1507C>A	ENSP00000326281.8:p.Pro503Thr
ENST00000349748.7:c.1507C>A	ENSP00000183936.4:p.Pro503Thr
ENST00000357568.7:c.1651C>A	ENSP00000350181.3:p.Pro551Thr
ENST00000397163.7:c.1651C>A	ENSP00000380349.3:p.Pro551Thr
ENST00000397200.8:c.115C>A	ENSP00000380384.4:p.Pro39Thr
ENST00000567071.5:c.110C>A
ENST00000569827.5:c.115C>A	ENSP00000454379.1:p.Pro39Thr
NM_000070.2:c.1651C>A	NP_000061.1:p.Pro551Thr
NM_024344.1:c.1651C>A	NP_077320.1:p.Pro551Thr
NM_173087.1:c.1507C>A	NP_775110.1:p.Pro503Thr
NM_173088.1:c.115C>A	NP_775111.1:p.Pro39Thr
NM_000070.3:c.1651C>A MANE Select	NP_000061.1:p.Pro551Thr
NM_024344.2:c.1651C>A	NP_077320.1:p.Pro551Thr
NM_173087.2:c.1507C>A	NP_775110.1:p.Pro503Thr
NM_173088.2:c.115C>A	NP_775111.1:p.Pro39Thr