Canonical Allele Identifier: CA10832576

Gene: CASP9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15515247G>A , CM000663.2:g.15515247G>A	GRCh38
NC_000001.10:g.15841742G>A , CM000663.1:g.15841742G>A	GRCh37
NC_000001.9:g.15714329G>A	NCBI36
NG_029188.1:g.14544C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333868.10:c.418+2863C>T MANE Select	ENSP00000330237.5:n.418+2863C>T
ENST00000333868.9:c.418+2863C>T	ENSP00000330237.5:n.418+2863C>T
ENST00000348549.9:c.418+2863C>T	ENSP00000255256.7:n.418+2863C>T
ENST00000375890.8:c.169+2863C>T	ENSP00000365051.4:n.169+2863C>T
ENST00000400777.7:c.410+2863C>T
ENST00000440484.1:c.418+2863C>T	ENSP00000411304.1:n.418+2863C>T
ENST00000447522.5:c.169+2863C>T	ENSP00000396540.1:n.169+2863C>T
ENST00000474305.2:c.278+3003C>T	ENSP00000449216.1:n.278+3003C>T
ENST00000546424.5:c.418+2863C>T	ENSP00000449584.1:n.418+2863C>T
ENST00000546969.1:n.433+2863C>T
NM_001229.4:c.418+2863C>T	NP_001220.2:n.418+2863C>T
NM_001278054.1:c.418+2863C>T	NP_001264983.1:n.418+2863C>T
NM_032996.3:c.169+2863C>T	NP_127463.2:n.169+2863C>T
NR_102732.1:n.663+2863C>T
NR_102733.1:n.523+3003C>T
XM_005246014.2:c.169+2863C>T	XP_005246071.1:n.169+2863C>T
XM_011542270.1:c.418+2863C>T	XP_011540572.1:n.418+2863C>T
XM_011542271.1:c.169+2863C>T	XP_011540573.1:n.169+2863C>T
XM_011542272.1:c.169+2863C>T	XP_011540574.1:n.169+2863C>T
XM_011542273.1:c.418+2863C>T	XP_011540575.1:n.418+2863C>T
XR_946778.1:n.583+2863C>T
XM_011542273.3:c.418+2863C>T	XP_011540575.1:n.418+2863C>T
NM_001229.5:c.418+2863C>T MANE Select	NP_001220.2:n.418+2863C>T
NM_001278054.2:c.418+2863C>T	NP_001264983.1:n.418+2863C>T
NR_102732.2:n.433+2863C>T
NR_102733.2:n.293+3003C>T