Canonical Allele Identifier: CA63865291
Gene: CASP10 HGNC NCBI

Linked Data

dbSNP Id: rs768371369

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201208170C>G , CM000664.2:g.201208170C>G GRCh38
NC_000002.11:g.202072893C>G , CM000664.1:g.202072893C>G GRCh37
NC_000002.10:g.201781138C>G NCBI36
NG_007265.1:g.30039C>G , LRG_33:g.30039C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.722-900C>G ENSP00000314599.7:n.722-900C>G
ENST00000346817.10:c.780C>G ENSP00000237865.7:p.Thr260=
ENST00000438843.6:c.*366C>G ENSP00000401914.1:n.*366C>G
ENST00000492363.6:c.817C>G ENSP00000512459.1:p.Pro273Ala
ENST00000696199.1:c.721+4404C>G ENSP00000512481.1:n.721+4404C>G
ENST00000286186.11:c.909C>G MANE Select ENSP00000286186.6:p.Thr303=
ENST00000272879.9:c.909C>G ENSP00000272879.5:p.Thr303=
ENST00000286186.10:c.909C>G ENSP00000286186.6:p.Thr303=
ENST00000313728.11:c.722-900C>G ENSP00000314599.7:n.722-900C>G
ENST00000346817.9:c.780C>G ENSP00000237865.7:p.Thr260=
ENST00000360132.7:c.817C>G ENSP00000353250.3:p.Pro273Ala
ENST00000448480.1:c.780C>G ENSP00000396835.1:p.Thr260=
ENST00000492363.5:n.817C>G
NM_001206524.1:c.722-900C>G NP_001193453.1:n.722-900C>G
NM_001206542.1:c.780C>G NP_001193471.1:p.Thr260=
NM_001230.4:c.780C>G NP_001221.2:p.Thr260=
NM_032974.4:c.909C>G NP_116756.2:p.Thr303=
NM_032976.3:c.817C>G NP_116758.1:p.Pro273Ala
NM_032977.3:c.909C>G , LRG_33t1:c.909C>G NP_116759.2:p.Thr303=
XM_005246907.2:c.906C>G XP_005246964.1:p.Thr302=
XM_006712796.2:c.159C>G XP_006712859.1:p.Thr53=
XM_011511990.1:c.814C>G XP_011510292.1:p.Pro272Ala
XR_923043.1:n.1113C>G
XR_923044.1:n.1021C>G
XM_006712796.3:c.159C>G XP_006712859.1:p.Thr53=
XM_011511990.2:c.814C>G XP_011510292.1:p.Pro272Ala
XR_923043.2:n.1113C>G
XR_923044.2:n.1021C>G
NM_001206524.2:c.722-900C>G NP_001193453.1:n.722-900C>G
NM_001206542.2:c.780C>G NP_001193471.1:p.Thr260=
NM_001230.5:c.780C>G NP_001221.2:p.Thr260=
NM_032974.5:c.909C>G NP_116756.2:p.Thr303=
NM_032977.4:c.909C>G MANE Select NP_116759.2:p.Thr303=
NM_032976.4:c.817C>G NP_116758.1:p.Pro273Ala