Canonical Allele Identifier: CA350286476
Gene: CASP10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201208133A>T , CM000664.2:g.201208133A>T GRCh38
NC_000002.11:g.202072856A>T , CM000664.1:g.202072856A>T GRCh37
NC_000002.10:g.201781101A>T NCBI36
NG_007265.1:g.30002A>T , LRG_33:g.30002A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.722-937A>T ENSP00000314599.7:n.722-937A>T
ENST00000346817.10:c.743A>T ENSP00000237865.7:p.Asn248Ile
ENST00000438843.6:c.*329A>T ENSP00000401914.1:n.*329A>T
ENST00000492363.6:c.780A>T ENSP00000512459.1:p.Gln260His
ENST00000696199.1:c.721+4367A>T ENSP00000512481.1:n.721+4367A>T
ENST00000286186.11:c.872A>T MANE Select ENSP00000286186.6:p.Asn291Ile
ENST00000272879.9:c.872A>T ENSP00000272879.5:p.Asn291Ile
ENST00000286186.10:c.872A>T ENSP00000286186.6:p.Asn291Ile
ENST00000313728.11:c.722-937A>T ENSP00000314599.7:n.722-937A>T
ENST00000346817.9:c.743A>T ENSP00000237865.7:p.Asn248Ile
ENST00000360132.7:c.780A>T ENSP00000353250.3:p.Gln260His
ENST00000438843.5:c.*329A>T ENSP00000401914.1:n.*329A>T
ENST00000448480.1:c.743A>T ENSP00000396835.1:p.Asn248Ile
ENST00000492363.5:n.780A>T
NM_001206524.1:c.722-937A>T NP_001193453.1:n.722-937A>T
NM_001206542.1:c.743A>T NP_001193471.1:p.Asn248Ile
NM_001230.4:c.743A>T NP_001221.2:p.Asn248Ile
NM_032974.4:c.872A>T NP_116756.2:p.Asn291Ile
NM_032976.3:c.780A>T NP_116758.1:p.Gln260His
NM_032977.3:c.872A>T , LRG_33t1:c.872A>T NP_116759.2:p.Asn291Ile
XM_005246907.2:c.869A>T XP_005246964.1:p.Asn290Ile
XM_006712796.2:c.122A>T XP_006712859.1:p.Asn41Ile
XM_011511990.1:c.777A>T XP_011510292.1:p.Gln259His
XR_923043.1:n.1076A>T
XR_923044.1:n.984A>T
XM_006712796.3:c.122A>T XP_006712859.1:p.Asn41Ile
XM_011511990.2:c.777A>T XP_011510292.1:p.Gln259His
XR_923043.2:n.1076A>T
XR_923044.2:n.984A>T
NM_001206524.2:c.722-937A>T NP_001193453.1:n.722-937A>T
NM_001206542.2:c.743A>T NP_001193471.1:p.Asn248Ile
NM_001230.5:c.743A>T NP_001221.2:p.Asn248Ile
NM_032974.5:c.872A>T NP_116756.2:p.Asn291Ile
NM_032977.4:c.872A>T MANE Select NP_116759.2:p.Asn291Ile
NM_032976.4:c.780A>T NP_116758.1:p.Gln260His