Canonical Allele Identifier: CA350286871
Gene: CASP10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201208163A>C , CM000664.2:g.201208163A>C GRCh38
NC_000002.11:g.202072886A>C , CM000664.1:g.202072886A>C GRCh37
NC_000002.10:g.201781131A>C NCBI36
NG_007265.1:g.30032A>C , LRG_33:g.30032A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.722-907A>C ENSP00000314599.7:n.722-907A>C
ENST00000346817.10:c.773A>C ENSP00000237865.7:p.Gln258Pro
ENST00000438843.6:c.*359A>C ENSP00000401914.1:n.*359A>C
ENST00000492363.6:c.810A>C ENSP00000512459.1:p.Thr270=
ENST00000696199.1:c.721+4397A>C ENSP00000512481.1:n.721+4397A>C
ENST00000286186.11:c.902A>C MANE Select ENSP00000286186.6:p.Gln301Pro
ENST00000272879.9:c.902A>C ENSP00000272879.5:p.Gln301Pro
ENST00000286186.10:c.902A>C ENSP00000286186.6:p.Gln301Pro
ENST00000313728.11:c.722-907A>C ENSP00000314599.7:n.722-907A>C
ENST00000346817.9:c.773A>C ENSP00000237865.7:p.Gln258Pro
ENST00000360132.7:c.810A>C ENSP00000353250.3:p.Thr270=
ENST00000448480.1:c.773A>C ENSP00000396835.1:p.Gln258Pro
ENST00000492363.5:n.810A>C
NM_001206524.1:c.722-907A>C NP_001193453.1:n.722-907A>C
NM_001206542.1:c.773A>C NP_001193471.1:p.Gln258Pro
NM_001230.4:c.773A>C NP_001221.2:p.Gln258Pro
NM_032974.4:c.902A>C NP_116756.2:p.Gln301Pro
NM_032976.3:c.810A>C NP_116758.1:p.Thr270=
NM_032977.3:c.902A>C , LRG_33t1:c.902A>C NP_116759.2:p.Gln301Pro
XM_005246907.2:c.899A>C XP_005246964.1:p.Gln300Pro
XM_006712796.2:c.152A>C XP_006712859.1:p.Gln51Pro
XM_011511990.1:c.807A>C XP_011510292.1:p.Thr269=
XR_923043.1:n.1106A>C
XR_923044.1:n.1014A>C
XM_006712796.3:c.152A>C XP_006712859.1:p.Gln51Pro
XM_011511990.2:c.807A>C XP_011510292.1:p.Thr269=
XR_923043.2:n.1106A>C
XR_923044.2:n.1014A>C
NM_001206524.2:c.722-907A>C NP_001193453.1:n.722-907A>C
NM_001206542.2:c.773A>C NP_001193471.1:p.Gln258Pro
NM_001230.5:c.773A>C NP_001221.2:p.Gln258Pro
NM_032974.5:c.902A>C NP_116756.2:p.Gln301Pro
NM_032977.4:c.902A>C MANE Select NP_116759.2:p.Gln301Pro
NM_032976.4:c.810A>C NP_116758.1:p.Thr270=