Canonical Allele Identifier: CA391995131

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 2203767
• ClinVar RCV Id: RCV002640761
• dbSNP Id: rs2052599999
• gnomAD v4: 15-42360071-A-G
• MyVariant Identifiers: chr15:g.42652269A>G (hg19) ; chr15:g.42360071A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42360071A>G , CM000677.2:g.42360071A>G	GRCh38
NC_000015.9:g.42652269A>G , CM000677.1:g.42652269A>G	GRCh37
NC_000015.8:g.40439561A>G	NCBI36
NG_008660.1:g.16969A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000349748.8:c.266A>G	ENSP00000183936.4:p.Tyr89Cys
ENST00000357568.8:c.266A>G	ENSP00000350181.3:p.Tyr89Cys
ENST00000397163.8:c.266A>G MANE Select	ENSP00000380349.3:p.Tyr89Cys
ENST00000466369.5:n.540+5618A>G
ENST00000483208.5:n.540+5618A>G
ENST00000495723.1:n.540+5618A>G
ENST00000549793.5:n.540+5618A>G
ENST00000318023.11:c.266A>G	ENSP00000326281.8:p.Tyr89Cys
ENST00000349748.7:c.266A>G	ENSP00000183936.4:p.Tyr89Cys
ENST00000357568.7:c.266A>G	ENSP00000350181.3:p.Tyr89Cys
ENST00000397163.7:c.266A>G	ENSP00000380349.3:p.Tyr89Cys
NM_000070.2:c.266A>G	NP_000061.1:p.Tyr89Cys
NM_024344.1:c.266A>G	NP_077320.1:p.Tyr89Cys
NM_173087.1:c.266A>G	NP_775110.1:p.Tyr89Cys
NM_000070.3:c.266A>G MANE Select	NP_000061.1:p.Tyr89Cys
NM_024344.2:c.266A>G	NP_077320.1:p.Tyr89Cys
NM_173087.2:c.266A>G	NP_775110.1:p.Tyr89Cys