Canonical Allele Identifier: CA2053202
Gene: CASP10 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 21727
dbSNP Id: rs13010627

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201209375G>A , CM000664.2:g.201209375G>A GRCh38
NC_000002.11:g.202074098G>A , CM000664.1:g.202074098G>A GRCh37
NC_000002.10:g.201782343G>A NCBI36
NG_007265.1:g.31244G>A , LRG_33:g.31244G>A

Transcript Alleles

HGVS Amino-acid change
NM_001206524.1:c.1027G>A VV NP_001193453.1:p.Val343Ile
NM_001206542.1:c.1099G>A VV NP_001193471.1:p.Val367Ile
NM_001230.4:c.1099G>A VV NP_001221.2:p.Val367Ile
NM_032974.4:c.1228G>A VV NP_116756.2:p.Val410Ile
NM_032976.3:c.*314G>A VV NP_116758.1:p.=
NM_032977.3:c.1228G>A , LRG_33t1:c.1228G>A NP_116759.2:p.Val410Ile
XM_005246907.2:c.1225G>A XP_005246964.1:p.Val409Ile
XM_006712796.2:c.478G>A XP_006712859.1:p.Val160Ile
XM_006712796.3:c.478G>A XP_006712859.1:p.Val160Ile
ENST00000272879.9:c.1228G>A ENSP00000272879.5:p.Val410Ile
ENST00000286186.10:c.1228G>A ENSP00000286186.6:p.Val410Ile
ENST00000313728.11:c.1027G>A ENSP00000314599.7:p.Val343Ile
ENST00000346817.9:c.1099G>A ENSP00000237865.7:p.Val367Ile
ENST00000360132.7:c.*314G>A ENSP00000353250.3:p.=
ENST00000448480.1:c.1099G>A ENSP00000396835.1:p.Val367Ile
ENST00000492363.5:n.1136G>A