Canonical Allele Identifier: CA2662631540

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201217584G>A , CM000664.2:g.201217584G>A	GRCh38
NC_000002.11:g.202082307G>A , CM000664.1:g.202082307G>A	GRCh37
NC_000002.10:g.201790552G>A	NCBI36
NG_007265.1:g.39453G>A , LRG_33:g.39453G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032977.4:c.1416-4G>A MANE Select	NP_116759.2:n.1416-4G>A
ENST00000286186.11:c.1416-4G>A MANE Select	ENSP00000286186.6:n.1416-4G>A
NM_001206524.1:c.1215-4G>A	NP_001193453.1:n.1215-4G>A
NM_001206524.2:c.1215-4G>A	NP_001193453.1:n.1215-4G>A
NM_001206542.1:c.1286+8022G>A	NP_001193471.1:n.1286+8022G>A
NM_001206542.2:c.1286+8022G>A	NP_001193471.1:n.1286+8022G>A
NM_001230.4:c.1287-4G>A	NP_001221.2:n.1287-4G>A
NM_001230.5:c.1287-4G>A	NP_001221.2:n.1287-4G>A
NM_032974.4:c.1415+8022G>A	NP_116756.2:n.1415+8022G>A
NM_032974.5:c.1415+8022G>A	NP_116756.2:n.1415+8022G>A
NM_032976.3:c.*502-4G>A	NP_116758.1:n.*502-4G>A
NM_032976.4:c.*502-4G>A	NP_116758.1:n.*502-4G>A
NM_032977.3:c.1416-4G>A , LRG_33t1:c.1416-4G>A	NP_116759.2:n.1416-4G>A
ENST00000272879.9:c.1415+8022G>A	ENSP00000272879.5:n.1415+8022G>A
ENST00000286186.10:c.1416-4G>A	ENSP00000286186.6:n.1416-4G>A
ENST00000313728.11:c.1215-4G>A	ENSP00000314599.7:n.1215-4G>A
ENST00000313728.12:c.1215-4G>A	ENSP00000314599.7:n.1215-4G>A
ENST00000346817.10:c.1287-4G>A	ENSP00000237865.7:n.1287-4G>A
ENST00000346817.9:c.1287-4G>A	ENSP00000237865.7:n.1287-4G>A
ENST00000360132.7:c.*502-4G>A	ENSP00000353250.3:n.*502-4G>A
ENST00000448480.1:c.1286+8022G>A	ENSP00000396835.1:n.1286+8022G>A
ENST00000492363.5:n.1324-4G>A
ENST00000492363.6:c.*502-4G>A	ENSP00000512459.1:n.*502-4G>A
ENST00000696199.1:c.722-11346G>A	ENSP00000512481.1:n.722-11346G>A
XM_005246907.2:c.1413-4G>A	XP_005246964.1:n.1413-4G>A
XM_006712796.2:c.666-4G>A	XP_006712859.1:n.666-4G>A
XM_006712796.3:c.666-4G>A	XP_006712859.1:n.666-4G>A