Canonical Allele Identifier: CA392000235

Gene: CAPN3

Linked Data

• MyVariant Identifiers: chr15:g.42695066C>G (hg19) ; chr15:g.42402868C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42402868C>G , CM000677.2:g.42402868C>G	GRCh38
NC_000015.9:g.42695066C>G , CM000677.1:g.42695066C>G	GRCh37
NC_000015.8:g.40482358C>G	NCBI36
NG_008660.1:g.59766C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.1467C>G	ENSP00000183936.4:p.Tyr489Ter
ENST00000357568.8:c.1611C>G	ENSP00000350181.3:p.Tyr537Ter
ENST00000397163.8:c.1611C>G MANE Select	ENSP00000380349.3:p.Tyr537Ter
ENST00000466369.5:n.2120C>G
ENST00000483208.5:n.2500C>G
ENST00000495723.1:n.2500C>G
ENST00000549793.5:n.1842C>G
ENST00000638141.2:n.1482C>G
ENST00000673646.1:c.75C>G	ENSP00000501007.1:p.Tyr25Ter
ENST00000673705.1:c.309+3216C>G	ENSP00000501021.1:n.309+3216C>G
ENST00000673813.1:n.533C>G
ENST00000318023.11:c.1467C>G	ENSP00000326281.8:p.Tyr489Ter
ENST00000349748.7:c.1467C>G	ENSP00000183936.4:p.Tyr489Ter
ENST00000357568.7:c.1611C>G	ENSP00000350181.3:p.Tyr537Ter
ENST00000397163.7:c.1611C>G	ENSP00000380349.3:p.Tyr537Ter
ENST00000397200.8:c.75C>G	ENSP00000380384.4:p.Tyr25Ter
ENST00000567071.5:c.70C>G
ENST00000569827.5:c.75C>G	ENSP00000454379.1:p.Tyr25Ter
NM_000070.2:c.1611C>G	NP_000061.1:p.Tyr537Ter
NM_024344.1:c.1611C>G	NP_077320.1:p.Tyr537Ter
NM_173087.1:c.1467C>G	NP_775110.1:p.Tyr489Ter
NM_173088.1:c.75C>G	NP_775111.1:p.Tyr25Ter
NM_000070.3:c.1611C>G MANE Select	NP_000061.1:p.Tyr537Ter
NM_024344.2:c.1611C>G	NP_077320.1:p.Tyr537Ter
NM_173087.2:c.1467C>G	NP_775110.1:p.Tyr489Ter
NM_173088.2:c.75C>G	NP_775111.1:p.Tyr25Ter