Canonical Allele Identifier: CA392000428

Gene: CAPN3

Linked Data

• MyVariant Identifiers: chr15:g.42695161T>G (hg19) ; chr15:g.42402963T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42402963T>G , CM000677.2:g.42402963T>G	GRCh38
NC_000015.9:g.42695161T>G , CM000677.1:g.42695161T>G	GRCh37
NC_000015.8:g.40482453T>G	NCBI36
NG_008660.1:g.59861T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1562T>G	ENSP00000183936.4:p.Phe521Cys
ENST00000357568.8:c.1706T>G	ENSP00000350181.3:p.Phe569Cys
ENST00000397163.8:c.1706T>G MANE Select	ENSP00000380349.3:p.Phe569Cys
ENST00000466369.5:n.2215T>G
ENST00000483208.5:n.2595T>G
ENST00000495723.1:n.2595T>G
ENST00000549793.5:n.1937T>G
ENST00000638141.2:n.1577T>G
ENST00000673646.1:c.170T>G	ENSP00000501007.1:p.Phe57Cys
ENST00000673705.1:c.309+3311T>G	ENSP00000501021.1:n.309+3311T>G
ENST00000673813.1:n.580+48T>G
ENST00000318023.11:c.1562T>G	ENSP00000326281.8:p.Phe521Cys
ENST00000349748.7:c.1562T>G	ENSP00000183936.4:p.Phe521Cys
ENST00000357568.7:c.1706T>G	ENSP00000350181.3:p.Phe569Cys
ENST00000397163.7:c.1706T>G	ENSP00000380349.3:p.Phe569Cys
ENST00000397200.8:c.170T>G	ENSP00000380384.4:p.Phe57Cys
ENST00000567071.5:c.165T>G
ENST00000569827.5:c.170T>G	ENSP00000454379.1:p.Phe57Cys
NM_000070.2:c.1706T>G	NP_000061.1:p.Phe569Cys
NM_024344.1:c.1706T>G	NP_077320.1:p.Phe569Cys
NM_173087.1:c.1562T>G	NP_775110.1:p.Phe521Cys
NM_173088.1:c.170T>G	NP_775111.1:p.Phe57Cys
NM_000070.3:c.1706T>G MANE Select	NP_000061.1:p.Phe569Cys
NM_024344.2:c.1706T>G	NP_077320.1:p.Phe569Cys
NM_173087.2:c.1562T>G	NP_775110.1:p.Phe521Cys
NM_173088.2:c.170T>G	NP_775111.1:p.Phe57Cys