Canonical Allele Identifier: CA2662631191

Gene: CASP10

Linked Data

• gnomAD v4: 2-201209523-T-TCATCTG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209523_201209524insCATCTG , CM000664.2:g.201209523_201209524insCATCTG	GRCh38
NC_000002.11:g.202074246_202074247insCATCTG , CM000664.1:g.202074246_202074247insCATCTG	GRCh37
NC_000002.10:g.201782491_201782492insCATCTG	NCBI36
NG_007265.1:g.31392_31393insCATCTG , LRG_33:g.31392_31393insCATCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1175_1176insCATCTG	ENSP00000314599.7:p.Ile392_Gln393insIleCys
ENST00000346817.10:c.1247_1248insCATCTG	ENSP00000237865.7:p.Ile416_Gln417insIleCys
ENST00000438843.6:c.*833_*834insCATCTG	ENSP00000401914.1:n.*833_*834insCATCTG
ENST00000492363.6:c.*462_*463insCATCTG	ENSP00000512459.1:n.*462_*463insCATCTG
ENST00000696199.1:c.721+5757_721+5758insCATCTG	ENSP00000512481.1:n.721+5757_721+5758insCATCTG
ENST00000286186.11:c.1376_1377insCATCTG MANE Select	ENSP00000286186.6:p.Ile459_Gln460insIleCys
ENST00000272879.9:c.1376_1377insCATCTG	ENSP00000272879.5:p.Ile459_Gln460insIleCys
ENST00000286186.10:c.1376_1377insCATCTG	ENSP00000286186.6:p.Ile459_Gln460insIleCys
ENST00000313728.11:c.1175_1176insCATCTG	ENSP00000314599.7:p.Ile392_Gln393insIleCys
ENST00000346817.9:c.1247_1248insCATCTG	ENSP00000237865.7:p.Ile416_Gln417insIleCys
ENST00000360132.7:c.*462_*463insCATCTG	ENSP00000353250.3:n.*462_*463insCATCTG
ENST00000448480.1:c.1247_1248insCATCTG	ENSP00000396835.1:p.Ile416_Gln417insIleCys
ENST00000492363.5:n.1284_1285insCATCTG
NM_001206524.1:c.1175_1176insCATCTG	NP_001193453.1:p.Ile392_Gln393insIleCys
NM_001206542.1:c.1247_1248insCATCTG	NP_001193471.1:p.Ile416_Gln417insIleCys
NM_001230.4:c.1247_1248insCATCTG	NP_001221.2:p.Ile416_Gln417insIleCys
NM_032974.4:c.1376_1377insCATCTG	NP_116756.2:p.Ile459_Gln460insIleCys
NM_032976.3:c.*462_*463insCATCTG	NP_116758.1:n.*462_*463insCATCTG
NM_032977.3:c.1376_1377insCATCTG , LRG_33t1:c.1376_1377insCATCTG	NP_116759.2:p.Ile459_Gln460insIleCys
XM_005246907.2:c.1373_1374insCATCTG	XP_005246964.1:p.Ile458_Gln459insIleCys
XM_006712796.2:c.626_627insCATCTG	XP_006712859.1:p.Ile209_Gln210insIleCys
XM_006712796.3:c.626_627insCATCTG	XP_006712859.1:p.Ile209_Gln210insIleCys
NM_001206524.2:c.1175_1176insCATCTG	NP_001193453.1:p.Ile392_Gln393insIleCys
NM_001206542.2:c.1247_1248insCATCTG	NP_001193471.1:p.Ile416_Gln417insIleCys
NM_001230.5:c.1247_1248insCATCTG	NP_001221.2:p.Ile416_Gln417insIleCys
NM_032974.5:c.1376_1377insCATCTG	NP_116756.2:p.Ile459_Gln460insIleCys
NM_032977.4:c.1376_1377insCATCTG MANE Select	NP_116759.2:p.Ile459_Gln460insIleCys
NM_032976.4:c.*462_*463insCATCTG	NP_116758.1:n.*462_*463insCATCTG