Canonical Allele Identifier: CA145726

Gene: CAPN3

Linked Data

• ClinVar Variation Id: 92420
• ClinVar RCV Id: RCV000078102 ; RCV000346923 ; RCV000399161 ; RCV000710095 ; RCV001526791
• dbSNP Id: rs1801449
• ExAC: 15:42681199 G / A
• gnomAD v2: 15-42681199-G-A
• gnomAD v3: 15-42389001-G-A
• gnomAD v4: 15-42389001-G-A
• MyVariant Identifiers: chr15:g.42681199G>A (hg19) ; chr15:g.42389001G>A (hg38)
• PubMed: PMID:10330340 ; PMID:19835634

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.42389001G>A , CM000677.2:g.42389001G>A	GRCh38
NC_000015.9:g.42681199G>A , CM000677.1:g.42681199G>A	GRCh37
NC_000015.8:g.40468491G>A	NCBI36
NG_008660.1:g.45899G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349748.8:c.706G>A	ENSP00000183936.4:p.Ala236Thr
ENST00000357568.8:c.706G>A	ENSP00000350181.3:p.Ala236Thr
ENST00000397163.8:c.706G>A MANE Select	ENSP00000380349.3:p.Ala236Thr
ENST00000466369.5:n.1215G>A
ENST00000483208.5:n.937G>A
ENST00000495723.1:n.937G>A
ENST00000549793.5:n.937G>A
ENST00000638141.2:n.721G>A
ENST00000673705.1:c.70+4449G>A	ENSP00000501021.1:n.70+4449G>A
ENST00000318023.11:c.706G>A	ENSP00000326281.8:p.Ala236Thr
ENST00000349748.7:c.706G>A	ENSP00000183936.4:p.Ala236Thr
ENST00000357568.7:c.706G>A	ENSP00000350181.3:p.Ala236Thr
ENST00000397163.7:c.706G>A	ENSP00000380349.3:p.Ala236Thr
NM_000070.2:c.706G>A	NP_000061.1:p.Ala236Thr
NM_024344.1:c.706G>A	NP_077320.1:p.Ala236Thr
NM_173087.1:c.706G>A	NP_775110.1:p.Ala236Thr
NM_000070.3:c.706G>A MANE Select	NP_000061.1:p.Ala236Thr
NM_024344.2:c.706G>A	NP_077320.1:p.Ala236Thr
NM_173087.2:c.706G>A	NP_775110.1:p.Ala236Thr