Canonical Allele Identifier: CA2701600546

Gene: CASP10

Linked Data

• dbSNP Id: rs2126041996

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201205973_201205974insA , CM000664.2:g.201205973_201205974insA	GRCh38
NC_000002.11:g.202070696_202070697insA , CM000664.1:g.202070696_202070697insA	GRCh37
NC_000002.10:g.201778941_201778942insA	NCBI36
NG_007265.1:g.27842_27843insA , LRG_33:g.27842_27843insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.721+2207_721+2208insA	ENSP00000314599.7:n.721+2207_721+2208insA
ENST00000346817.10:c.685-2102_685-2101insA	ENSP00000237865.7:n.685-2102_685-2101insA
ENST00000438843.6:c.*271-2102_*271-2101insA	ENSP00000401914.1:n.*271-2102_*271-2101insA
ENST00000492363.6:c.722-2102_722-2101insA	ENSP00000512459.1:n.722-2102_722-2101insA
ENST00000696199.1:c.721+2207_721+2208insA	ENSP00000512481.1:n.721+2207_721+2208insA
ENST00000286186.11:c.813_813+1insA MANE Select	ENSP00000286186.6:n.813_813+1insA
ENST00000272879.9:c.813_813+1insA	ENSP00000272879.5:n.813_813+1insA
ENST00000286186.10:c.813_813+1insA	ENSP00000286186.6:n.813_813+1insA
ENST00000313728.11:c.721+2207_721+2208insA	ENSP00000314599.7:n.721+2207_721+2208insA
ENST00000346817.9:c.685-2102_685-2101insA	ENSP00000237865.7:n.685-2102_685-2101insA
ENST00000360132.7:c.722-2102_722-2101insA	ENSP00000353250.3:n.722-2102_722-2101insA
ENST00000438843.5:c.*271-2102_*271-2101insA	ENSP00000401914.1:n.*271-2102_*271-2101insA
ENST00000448480.1:c.685-2102_685-2101insA	ENSP00000396835.1:n.685-2102_685-2101insA
ENST00000460140.5:n.1017_1018insA
ENST00000492363.5:n.722-2102_722-2101insA
NM_001206524.1:c.721+2207_721+2208insA	NP_001193453.1:n.721+2207_721+2208insA
NM_001206542.1:c.685-2102_685-2101insA	NP_001193471.1:n.685-2102_685-2101insA
NM_001230.4:c.685-2102_685-2101insA	NP_001221.2:n.685-2102_685-2101insA
NM_032974.4:c.813_813+1insA	NP_116756.2:n.813_813+1insA
NM_032976.3:c.722-2102_722-2101insA	NP_116758.1:n.722-2102_722-2101insA
NM_032977.3:c.813_813+1insA , LRG_33t1:c.813_813+1insA	NP_116759.2:n.813_813+1insA
XM_005246907.2:c.810_810+1insA	XP_005246964.1:n.810_810+1insA
XM_006712796.2:c.64-2102_64-2101insA	XP_006712859.1:n.64-2102_64-2101insA
XM_011511990.1:c.719-2102_719-2101insA	XP_011510292.1:n.719-2102_719-2101insA
XR_923043.1:n.1017_1017+1insA
XR_923044.1:n.926-2102_926-2101insA
XM_006712796.3:c.64-2102_64-2101insA	XP_006712859.1:n.64-2102_64-2101insA
XM_011511990.2:c.719-2102_719-2101insA	XP_011510292.1:n.719-2102_719-2101insA
XR_923043.2:n.1017_1017+1insA
XR_923044.2:n.926-2102_926-2101insA
NM_001206524.2:c.721+2207_721+2208insA	NP_001193453.1:n.721+2207_721+2208insA
NM_001206542.2:c.685-2102_685-2101insA	NP_001193471.1:n.685-2102_685-2101insA
NM_001230.5:c.685-2102_685-2101insA	NP_001221.2:n.685-2102_685-2101insA
NM_032974.5:c.813_813+1insA	NP_116756.2:n.813_813+1insA
NM_032977.4:c.813_813+1insA MANE Select	NP_116759.2:n.813_813+1insA
NM_032976.4:c.722-2102_722-2101insA	NP_116758.1:n.722-2102_722-2101insA