Canonical Allele Identifier: CA1320965846

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201206012_201206013delinsAT , CM000664.2:g.201206012_201206013delinsAT	GRCh38
NC_000002.11:g.202070735_202070736delinsAT , CM000664.1:g.202070735_202070736delinsAT	GRCh37
NC_000002.10:g.201778980_201778981delinsAT	NCBI36
NG_007265.1:g.27881_27882delinsAT , LRG_33:g.27881_27882delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.721+2246_721+2247delinsAT	ENSP00000314599.7:n.721+2246_721+2247delinsAT
ENST00000346817.10:c.685-2063_685-2062delinsAT	ENSP00000237865.7:n.685-2063_685-2062delinsAT
ENST00000438843.6:c.*271-2063_*271-2062delinsAT	ENSP00000401914.1:n.*271-2063_*271-2062delinsAT
ENST00000492363.6:c.722-2063_722-2062delinsAT	ENSP00000512459.1:n.722-2063_722-2062delinsAT
ENST00000696199.1:c.721+2246_721+2247delinsAT	ENSP00000512481.1:n.721+2246_721+2247delinsAT
ENST00000286186.11:c.813+39_813+40delinsAT MANE Select	ENSP00000286186.6:n.813+39_813+40delinsAT
ENST00000272879.9:c.813+39_813+40delinsAT	ENSP00000272879.5:n.813+39_813+40delinsAT
ENST00000286186.10:c.813+39_813+40delinsAT	ENSP00000286186.6:n.813+39_813+40delinsAT
ENST00000313728.11:c.721+2246_721+2247delinsAT	ENSP00000314599.7:n.721+2246_721+2247delinsAT
ENST00000346817.9:c.685-2063_685-2062delinsAT	ENSP00000237865.7:n.685-2063_685-2062delinsAT
ENST00000360132.7:c.722-2063_722-2062delinsAT	ENSP00000353250.3:n.722-2063_722-2062delinsAT
ENST00000438843.5:c.*271-2063_*271-2062delinsAT	ENSP00000401914.1:n.*271-2063_*271-2062delinsAT
ENST00000448480.1:c.685-2063_685-2062delinsAT	ENSP00000396835.1:n.685-2063_685-2062delinsAT
ENST00000460140.5:n.1056_1057delinsAT
ENST00000492363.5:n.722-2063_722-2062delinsAT
NM_001206524.1:c.721+2246_721+2247delinsAT	NP_001193453.1:n.721+2246_721+2247delinsAT
NM_001206542.1:c.685-2063_685-2062delinsAT	NP_001193471.1:n.685-2063_685-2062delinsAT
NM_001230.4:c.685-2063_685-2062delinsAT	NP_001221.2:n.685-2063_685-2062delinsAT
NM_032974.4:c.813+39_813+40delinsAT	NP_116756.2:n.813+39_813+40delinsAT
NM_032976.3:c.722-2063_722-2062delinsAT	NP_116758.1:n.722-2063_722-2062delinsAT
NM_032977.3:c.813+39_813+40delinsAT , LRG_33t1:c.813+39_813+40delinsAT	NP_116759.2:n.813+39_813+40delinsAT
XM_005246907.2:c.810+39_810+40delinsAT	XP_005246964.1:n.810+39_810+40delinsAT
XM_006712796.2:c.64-2063_64-2062delinsAT	XP_006712859.1:n.64-2063_64-2062delinsAT
XM_011511990.1:c.719-2063_719-2062delinsAT	XP_011510292.1:n.719-2063_719-2062delinsAT
XR_923043.1:n.1017+39_1017+40delinsAT
XR_923044.1:n.926-2063_926-2062delinsAT
XM_006712796.3:c.64-2063_64-2062delinsAT	XP_006712859.1:n.64-2063_64-2062delinsAT
XM_011511990.2:c.719-2063_719-2062delinsAT	XP_011510292.1:n.719-2063_719-2062delinsAT
XR_923043.2:n.1017+39_1017+40delinsAT
XR_923044.2:n.926-2063_926-2062delinsAT
NM_001206524.2:c.721+2246_721+2247delinsAT	NP_001193453.1:n.721+2246_721+2247delinsAT
NM_001206542.2:c.685-2063_685-2062delinsAT	NP_001193471.1:n.685-2063_685-2062delinsAT
NM_001230.5:c.685-2063_685-2062delinsAT	NP_001221.2:n.685-2063_685-2062delinsAT
NM_032974.5:c.813+39_813+40delinsAT	NP_116756.2:n.813+39_813+40delinsAT
NM_032977.4:c.813+39_813+40delinsAT MANE Select	NP_116759.2:n.813+39_813+40delinsAT
NM_032976.4:c.722-2063_722-2062delinsAT	NP_116758.1:n.722-2063_722-2062delinsAT