Canonical Allele Identifier: CA2662631189

Gene: CASP10

Linked Data

• gnomAD v4: 2-201209517-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209517_201209518insT , CM000664.2:g.201209517_201209518insT	GRCh38
NC_000002.11:g.202074240_202074241insT , CM000664.1:g.202074240_202074241insT	GRCh37
NC_000002.10:g.201782485_201782486insT	NCBI36
NG_007265.1:g.31386_31387insT , LRG_33:g.31386_31387insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1169_1170insT	ENSP00000314599.7:p.Trp390CysfsTer8
ENST00000346817.10:c.1241_1242insT	ENSP00000237865.7:p.Trp414CysfsTer8
ENST00000438843.6:c.*827_*828insT	ENSP00000401914.1:n.*827_*828insT
ENST00000492363.6:c.*456_*457insT	ENSP00000512459.1:n.*456_*457insT
ENST00000696199.1:c.721+5751_721+5752insT	ENSP00000512481.1:n.721+5751_721+5752insT
ENST00000286186.11:c.1370_1371insT MANE Select	ENSP00000286186.6:p.Trp457CysfsTer8
ENST00000272879.9:c.1370_1371insT	ENSP00000272879.5:p.Trp457CysfsTer8
ENST00000286186.10:c.1370_1371insT	ENSP00000286186.6:p.Trp457CysfsTer8
ENST00000313728.11:c.1169_1170insT	ENSP00000314599.7:p.Trp390CysfsTer8
ENST00000346817.9:c.1241_1242insT	ENSP00000237865.7:p.Trp414CysfsTer8
ENST00000360132.7:c.*456_*457insT	ENSP00000353250.3:n.*456_*457insT
ENST00000448480.1:c.1241_1242insT	ENSP00000396835.1:p.Trp414CysfsTer8
ENST00000492363.5:n.1278_1279insT
NM_001206524.1:c.1169_1170insT	NP_001193453.1:p.Trp390CysfsTer8
NM_001206542.1:c.1241_1242insT	NP_001193471.1:p.Trp414CysfsTer8
NM_001230.4:c.1241_1242insT	NP_001221.2:p.Trp414CysfsTer8
NM_032974.4:c.1370_1371insT	NP_116756.2:p.Trp457CysfsTer8
NM_032976.3:c.*456_*457insT	NP_116758.1:n.*456_*457insT
NM_032977.3:c.1370_1371insT , LRG_33t1:c.1370_1371insT	NP_116759.2:p.Trp457CysfsTer8
XM_005246907.2:c.1367_1368insT	XP_005246964.1:p.Trp456CysfsTer8
XM_006712796.2:c.620_621insT	XP_006712859.1:p.Trp207CysfsTer8
XM_006712796.3:c.620_621insT	XP_006712859.1:p.Trp207CysfsTer8
NM_001206524.2:c.1169_1170insT	NP_001193453.1:p.Trp390CysfsTer8
NM_001206542.2:c.1241_1242insT	NP_001193471.1:p.Trp414CysfsTer8
NM_001230.5:c.1241_1242insT	NP_001221.2:p.Trp414CysfsTer8
NM_032974.5:c.1370_1371insT	NP_116756.2:p.Trp457CysfsTer8
NM_032977.4:c.1370_1371insT MANE Select	NP_116759.2:p.Trp457CysfsTer8
NM_032976.4:c.*456_*457insT	NP_116758.1:n.*456_*457insT