Canonical Allele Identifier: CA1320967428

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209564_201209566delinsTGA , CM000664.2:g.201209564_201209566delinsTGA	GRCh38
NC_000002.11:g.202074287_202074289delinsTGA , CM000664.1:g.202074287_202074289delinsTGA	GRCh37
NC_000002.10:g.201782532_201782534delinsTGA	NCBI36
NG_007265.1:g.31433_31435delinsTGA , LRG_33:g.31433_31435delinsTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1214+2_1214+4delinsTGA	ENSP00000314599.7:n.1214+2_1214+4delinsTGA
ENST00000346817.10:c.1286+2_1286+4delinsTGA	ENSP00000237865.7:n.1286+2_1286+4delinsTGA
ENST00000492363.6:c.*501+2_*501+4delinsTGA	ENSP00000512459.1:n.*501+2_*501+4delinsTGA
ENST00000696199.1:c.721+5798_721+5800delinsTGA	ENSP00000512481.1:n.721+5798_721+5800delinsTGA
ENST00000286186.11:c.1415+2_1415+4delinsTGA MANE Select	ENSP00000286186.6:n.1415+2_1415+4delinsTGA
ENST00000272879.9:c.1415+2_1415+4delinsTGA	ENSP00000272879.5:n.1415+2_1415+4delinsTGA
ENST00000286186.10:c.1415+2_1415+4delinsTGA	ENSP00000286186.6:n.1415+2_1415+4delinsTGA
ENST00000313728.11:c.1214+2_1214+4delinsTGA	ENSP00000314599.7:n.1214+2_1214+4delinsTGA
ENST00000346817.9:c.1286+2_1286+4delinsTGA	ENSP00000237865.7:n.1286+2_1286+4delinsTGA
ENST00000360132.7:c.*501+2_*501+4delinsTGA	ENSP00000353250.3:n.*501+2_*501+4delinsTGA
ENST00000448480.1:c.1286+2_1286+4delinsTGA	ENSP00000396835.1:n.1286+2_1286+4delinsTGA
ENST00000492363.5:n.1323+2_1323+4delinsTGA
NM_001206524.1:c.1214+2_1214+4delinsTGA	NP_001193453.1:n.1214+2_1214+4delinsTGA
NM_001206542.1:c.1286+2_1286+4delinsTGA	NP_001193471.1:n.1286+2_1286+4delinsTGA
NM_001230.4:c.1286+2_1286+4delinsTGA	NP_001221.2:n.1286+2_1286+4delinsTGA
NM_032974.4:c.1415+2_1415+4delinsTGA	NP_116756.2:n.1415+2_1415+4delinsTGA
NM_032976.3:c.*501+2_*501+4delinsTGA	NP_116758.1:n.*501+2_*501+4delinsTGA
NM_032977.3:c.1415+2_1415+4delinsTGA , LRG_33t1:c.1415+2_1415+4delinsTGA	NP_116759.2:n.1415+2_1415+4delinsTGA
XM_005246907.2:c.1412+2_1412+4delinsTGA	XP_005246964.1:n.1412+2_1412+4delinsTGA
XM_006712796.2:c.665+2_665+4delinsTGA	XP_006712859.1:n.665+2_665+4delinsTGA
XM_006712796.3:c.665+2_665+4delinsTGA	XP_006712859.1:n.665+2_665+4delinsTGA
NM_001206524.2:c.1214+2_1214+4delinsTGA	NP_001193453.1:n.1214+2_1214+4delinsTGA
NM_001206542.2:c.1286+2_1286+4delinsTGA	NP_001193471.1:n.1286+2_1286+4delinsTGA
NM_001230.5:c.1286+2_1286+4delinsTGA	NP_001221.2:n.1286+2_1286+4delinsTGA
NM_032974.5:c.1415+2_1415+4delinsTGA	NP_116756.2:n.1415+2_1415+4delinsTGA
NM_032977.4:c.1415+2_1415+4delinsTGA MANE Select	NP_116759.2:n.1415+2_1415+4delinsTGA
NM_032976.4:c.*501+2_*501+4delinsTGA	NP_116758.1:n.*501+2_*501+4delinsTGA