Canonical Allele Identifier: CA2662631180

Gene: CASP10

Linked Data

• gnomAD v4: 2-201209162-CAGAAGTGCAATCCAGCCCATGCCGACGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209163_201209190del , CM000664.2:g.201209163_201209190del	GRCh38
NC_000002.11:g.202073886_202073913del , CM000664.1:g.202073886_202073913del	GRCh37
NC_000002.10:g.201782131_201782158del	NCBI36
NG_007265.1:g.31032_31059del , LRG_33:g.31032_31059del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.815_842del	ENSP00000314599.7:p.Gln272ArgfsTer9
ENST00000346817.10:c.887_914del	ENSP00000237865.7:p.Gln296ArgfsTer9
ENST00000438843.6:c.*473_*500del	ENSP00000401914.1:n.*473_*500del
ENST00000492363.6:c.*102_*129del	ENSP00000512459.1:n.*102_*129del
ENST00000696199.1:c.721+5397_721+5424del	ENSP00000512481.1:n.721+5397_721+5424del
ENST00000286186.11:c.1016_1043del MANE Select	ENSP00000286186.6:p.Gln339ArgfsTer9
ENST00000272879.9:c.1016_1043del	ENSP00000272879.5:p.Gln339ArgfsTer9
ENST00000286186.10:c.1016_1043del	ENSP00000286186.6:p.Gln339ArgfsTer9
ENST00000313728.11:c.815_842del	ENSP00000314599.7:p.Gln272ArgfsTer9
ENST00000346817.9:c.887_914del	ENSP00000237865.7:p.Gln296ArgfsTer9
ENST00000360132.7:c.*102_*129del	ENSP00000353250.3:n.*102_*129del
ENST00000448480.1:c.887_914del	ENSP00000396835.1:p.Gln296ArgfsTer9
ENST00000492363.5:n.924_951del
NM_001206524.1:c.815_842del	NP_001193453.1:p.Gln272ArgfsTer9
NM_001206542.1:c.887_914del	NP_001193471.1:p.Gln296ArgfsTer9
NM_001230.4:c.887_914del	NP_001221.2:p.Gln296ArgfsTer9
NM_032974.4:c.1016_1043del	NP_116756.2:p.Gln339ArgfsTer9
NM_032976.3:c.*102_*129del	NP_116758.1:n.*102_*129del
NM_032977.3:c.1016_1043del , LRG_33t1:c.1016_1043del	NP_116759.2:p.Gln339ArgfsTer9
XM_005246907.2:c.1013_1040del	XP_005246964.1:p.Gln338ArgfsTer9
XM_006712796.2:c.266_293del	XP_006712859.1:p.Gln89ArgfsTer9
XM_006712796.3:c.266_293del	XP_006712859.1:p.Gln89ArgfsTer9
NM_001206524.2:c.815_842del	NP_001193453.1:p.Gln272ArgfsTer9
NM_001206542.2:c.887_914del	NP_001193471.1:p.Gln296ArgfsTer9
NM_001230.5:c.887_914del	NP_001221.2:p.Gln296ArgfsTer9
NM_032974.5:c.1016_1043del	NP_116756.2:p.Gln339ArgfsTer9
NM_032977.4:c.1016_1043del MANE Select	NP_116759.2:p.Gln339ArgfsTer9
NM_032976.4:c.*102_*129del	NP_116758.1:n.*102_*129del