Canonical Allele Identifier: CA350286432
Gene: CASP10 HGNC NCBI

Linked Data

dbSNP Id: rs1157122824

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201208129A>G , CM000664.2:g.201208129A>G GRCh38
NC_000002.11:g.202072852A>G , CM000664.1:g.202072852A>G GRCh37
NC_000002.10:g.201781097A>G NCBI36
NG_007265.1:g.29998A>G , LRG_33:g.29998A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.722-941A>G ENSP00000314599.7:n.722-941A>G
ENST00000346817.10:c.739A>G ENSP00000237865.7:p.Asn247Asp
ENST00000438843.6:c.*325A>G ENSP00000401914.1:n.*325A>G
ENST00000492363.6:c.776A>G ENSP00000512459.1:p.Gln259Arg
ENST00000696199.1:c.721+4363A>G ENSP00000512481.1:n.721+4363A>G
ENST00000286186.11:c.868A>G MANE Select ENSP00000286186.6:p.Asn290Asp
ENST00000272879.9:c.868A>G ENSP00000272879.5:p.Asn290Asp
ENST00000286186.10:c.868A>G ENSP00000286186.6:p.Asn290Asp
ENST00000313728.11:c.722-941A>G ENSP00000314599.7:n.722-941A>G
ENST00000346817.9:c.739A>G ENSP00000237865.7:p.Asn247Asp
ENST00000360132.7:c.776A>G ENSP00000353250.3:p.Gln259Arg
ENST00000438843.5:c.*325A>G ENSP00000401914.1:n.*325A>G
ENST00000448480.1:c.739A>G ENSP00000396835.1:p.Asn247Asp
ENST00000492363.5:n.776A>G
NM_001206524.1:c.722-941A>G NP_001193453.1:n.722-941A>G
NM_001206542.1:c.739A>G NP_001193471.1:p.Asn247Asp
NM_001230.4:c.739A>G NP_001221.2:p.Asn247Asp
NM_032974.4:c.868A>G NP_116756.2:p.Asn290Asp
NM_032976.3:c.776A>G NP_116758.1:p.Gln259Arg
NM_032977.3:c.868A>G , LRG_33t1:c.868A>G NP_116759.2:p.Asn290Asp
XM_005246907.2:c.865A>G XP_005246964.1:p.Asn289Asp
XM_006712796.2:c.118A>G XP_006712859.1:p.Asn40Asp
XM_011511990.1:c.773A>G XP_011510292.1:p.Gln258Arg
XR_923043.1:n.1072A>G
XR_923044.1:n.980A>G
XM_006712796.3:c.118A>G XP_006712859.1:p.Asn40Asp
XM_011511990.2:c.773A>G XP_011510292.1:p.Gln258Arg
XR_923043.2:n.1072A>G
XR_923044.2:n.980A>G
NM_001206524.2:c.722-941A>G NP_001193453.1:n.722-941A>G
NM_001206542.2:c.739A>G NP_001193471.1:p.Asn247Asp
NM_001230.5:c.739A>G NP_001221.2:p.Asn247Asp
NM_032974.5:c.868A>G NP_116756.2:p.Asn290Asp
NM_032977.4:c.868A>G MANE Select NP_116759.2:p.Asn290Asp
NM_032976.4:c.776A>G NP_116758.1:p.Gln259Arg