Canonical Allele Identifier: CA350286391
Gene: CASP10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201208125T>A , CM000664.2:g.201208125T>A GRCh38
NC_000002.11:g.202072848T>A , CM000664.1:g.202072848T>A GRCh37
NC_000002.10:g.201781093T>A NCBI36
NG_007265.1:g.29994T>A , LRG_33:g.29994T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.722-945T>A ENSP00000314599.7:n.722-945T>A
ENST00000346817.10:c.735T>A ENSP00000237865.7:p.Ile245=
ENST00000438843.6:c.*321T>A ENSP00000401914.1:n.*321T>A
ENST00000492363.6:c.772T>A ENSP00000512459.1:p.Cys258Ser
ENST00000696199.1:c.721+4359T>A ENSP00000512481.1:n.721+4359T>A
ENST00000286186.11:c.864T>A MANE Select ENSP00000286186.6:p.Ile288=
ENST00000272879.9:c.864T>A ENSP00000272879.5:p.Ile288=
ENST00000286186.10:c.864T>A ENSP00000286186.6:p.Ile288=
ENST00000313728.11:c.722-945T>A ENSP00000314599.7:n.722-945T>A
ENST00000346817.9:c.735T>A ENSP00000237865.7:p.Ile245=
ENST00000360132.7:c.772T>A ENSP00000353250.3:p.Cys258Ser
ENST00000438843.5:c.*321T>A ENSP00000401914.1:n.*321T>A
ENST00000448480.1:c.735T>A ENSP00000396835.1:p.Ile245=
ENST00000492363.5:n.772T>A
NM_001206524.1:c.722-945T>A NP_001193453.1:n.722-945T>A
NM_001206542.1:c.735T>A NP_001193471.1:p.Ile245=
NM_001230.4:c.735T>A NP_001221.2:p.Ile245=
NM_032974.4:c.864T>A NP_116756.2:p.Ile288=
NM_032976.3:c.772T>A NP_116758.1:p.Cys258Ser
NM_032977.3:c.864T>A , LRG_33t1:c.864T>A NP_116759.2:p.Ile288=
XM_005246907.2:c.861T>A XP_005246964.1:p.Ile287=
XM_006712796.2:c.114T>A XP_006712859.1:p.Ile38=
XM_011511990.1:c.769T>A XP_011510292.1:p.Cys257Ser
XR_923043.1:n.1068T>A
XR_923044.1:n.976T>A
XM_006712796.3:c.114T>A XP_006712859.1:p.Ile38=
XM_011511990.2:c.769T>A XP_011510292.1:p.Cys257Ser
XR_923043.2:n.1068T>A
XR_923044.2:n.976T>A
NM_001206524.2:c.722-945T>A NP_001193453.1:n.722-945T>A
NM_001206542.2:c.735T>A NP_001193471.1:p.Ile245=
NM_001230.5:c.735T>A NP_001221.2:p.Ile245=
NM_032974.5:c.864T>A NP_116756.2:p.Ile288=
NM_032977.4:c.864T>A MANE Select NP_116759.2:p.Ile288=
NM_032976.4:c.772T>A NP_116758.1:p.Cys258Ser