Canonical Allele Identifier: CA350286855
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2931869
ClinVar RCV Id: RCV003792891

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201208162C>G , CM000664.2:g.201208162C>G GRCh38
NC_000002.11:g.202072885C>G , CM000664.1:g.202072885C>G GRCh37
NC_000002.10:g.201781130C>G NCBI36
NG_007265.1:g.30031C>G , LRG_33:g.30031C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.722-908C>G ENSP00000314599.7:n.722-908C>G
ENST00000346817.10:c.772C>G ENSP00000237865.7:p.Gln258Glu
ENST00000438843.6:c.*358C>G ENSP00000401914.1:n.*358C>G
ENST00000492363.6:c.809C>G ENSP00000512459.1:p.Thr270Arg
ENST00000696199.1:c.721+4396C>G ENSP00000512481.1:n.721+4396C>G
ENST00000286186.11:c.901C>G MANE Select ENSP00000286186.6:p.Gln301Glu
ENST00000272879.9:c.901C>G ENSP00000272879.5:p.Gln301Glu
ENST00000286186.10:c.901C>G ENSP00000286186.6:p.Gln301Glu
ENST00000313728.11:c.722-908C>G ENSP00000314599.7:n.722-908C>G
ENST00000346817.9:c.772C>G ENSP00000237865.7:p.Gln258Glu
ENST00000360132.7:c.809C>G ENSP00000353250.3:p.Thr270Arg
ENST00000448480.1:c.772C>G ENSP00000396835.1:p.Gln258Glu
ENST00000492363.5:n.809C>G
NM_001206524.1:c.722-908C>G NP_001193453.1:n.722-908C>G
NM_001206542.1:c.772C>G NP_001193471.1:p.Gln258Glu
NM_001230.4:c.772C>G NP_001221.2:p.Gln258Glu
NM_032974.4:c.901C>G NP_116756.2:p.Gln301Glu
NM_032976.3:c.809C>G NP_116758.1:p.Thr270Arg
NM_032977.3:c.901C>G , LRG_33t1:c.901C>G NP_116759.2:p.Gln301Glu
XM_005246907.2:c.898C>G XP_005246964.1:p.Gln300Glu
XM_006712796.2:c.151C>G XP_006712859.1:p.Gln51Glu
XM_011511990.1:c.806C>G XP_011510292.1:p.Thr269Arg
XR_923043.1:n.1105C>G
XR_923044.1:n.1013C>G
XM_006712796.3:c.151C>G XP_006712859.1:p.Gln51Glu
XM_011511990.2:c.806C>G XP_011510292.1:p.Thr269Arg
XR_923043.2:n.1105C>G
XR_923044.2:n.1013C>G
NM_001206524.2:c.722-908C>G NP_001193453.1:n.722-908C>G
NM_001206542.2:c.772C>G NP_001193471.1:p.Gln258Glu
NM_001230.5:c.772C>G NP_001221.2:p.Gln258Glu
NM_032974.5:c.901C>G NP_116756.2:p.Gln301Glu
NM_032977.4:c.901C>G MANE Select NP_116759.2:p.Gln301Glu
NM_032976.4:c.809C>G NP_116758.1:p.Thr270Arg