Canonical Allele Identifier: CA1320967267
Gene: CASP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201209201G= , CM000664.2:g.201209201G= GRCh38
NC_000002.11:g.202073924G= , CM000664.1:g.202073924G= GRCh37
NC_000002.10:g.201782169G= NCBI36
NG_007265.1:g.31070G= , LRG_33:g.31070G=

Transcript Alleles

HGVS Amino-acid change
ENST00000313728.12:c.853G= ENSP00000314599.7:p.Val285=
ENST00000346817.10:c.925G= ENSP00000237865.7:p.Val309=
ENST00000438843.6:c.*511G= ENSP00000401914.1:n.*511G=
ENST00000492363.6:c.*140G= ENSP00000512459.1:n.*140G=
ENST00000696199.1:c.721+5435G= ENSP00000512481.1:n.721+5435G=
ENST00000286186.11:c.1054G= MANE Select ENSP00000286186.6:p.Val352=
ENST00000272879.9:c.1054G= ENSP00000272879.5:p.Val352=
ENST00000286186.10:c.1054G= ENSP00000286186.6:p.Val352=
ENST00000313728.11:c.853G= ENSP00000314599.7:p.Val285=
ENST00000346817.9:c.925G= ENSP00000237865.7:p.Val309=
ENST00000360132.7:c.*140G= ENSP00000353250.3:n.*140G=
ENST00000448480.1:c.925G= ENSP00000396835.1:p.Val309=
ENST00000492363.5:n.962G=
NM_001206524.1:c.853G= NP_001193453.1:p.Val285=
NM_001206542.1:c.925G= NP_001193471.1:p.Val309=
NM_001230.4:c.925G= NP_001221.2:p.Val309=
NM_032974.4:c.1054G= NP_116756.2:p.Val352=
NM_032976.3:c.*140G= NP_116758.1:n.*140G=
NM_032977.3:c.1054G= , LRG_33t1:c.1054G= NP_116759.2:p.Val352=
XM_005246907.2:c.1051G= XP_005246964.1:p.Val351=
XM_006712796.2:c.304G= XP_006712859.1:p.Val102=
XM_006712796.3:c.304G= XP_006712859.1:p.Val102=
NM_001206524.2:c.853G= NP_001193453.1:p.Val285=
NM_001206542.2:c.925G= NP_001193471.1:p.Val309=
NM_001230.5:c.925G= NP_001221.2:p.Val309=
NM_032974.5:c.1054G= NP_116756.2:p.Val352=
NM_032977.4:c.1054G= MANE Select NP_116759.2:p.Val352=
NM_032976.4:c.*140G= NP_116758.1:n.*140G=