Canonical Allele Identifier: CA1140030957

Gene: CASP9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15506705C= , CM000663.2:g.15506705C=	GRCh38
NC_000001.10:g.15833200C= , CM000663.1:g.15833200C=	GRCh37
NC_000001.9:g.15705787C=	NCBI36
NG_029188.1:g.23086G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333868.10:c.630+194G= MANE Select	ENSP00000330237.5:n.630+194G=
ENST00000333868.9:c.630+194G=	ENSP00000330237.5:n.630+194G=
ENST00000348549.9:c.419-11253G=	ENSP00000255256.7:n.419-11253G=
ENST00000375890.8:c.381+194G=	ENSP00000365051.4:n.381+194G=
ENST00000400777.7:c.680+194G=
ENST00000424908.5:c.154+194G=
ENST00000440484.1:c.630+194G=	ENSP00000411304.1:n.630+194G=
ENST00000447522.5:c.381+194G=	ENSP00000396540.1:n.381+194G=
ENST00000474305.2:c.490+194G=	ENSP00000449216.1:n.490+194G=
ENST00000546424.5:c.630+194G=	ENSP00000449584.1:n.630+194G=
NM_001229.4:c.630+194G=	NP_001220.2:n.630+194G=
NM_001278054.1:c.419-11253G=	NP_001264983.1:n.419-11253G=
NM_032996.3:c.381+194G=	NP_127463.2:n.381+194G=
NR_102732.1:n.933+194G=
NR_102733.1:n.735+194G=
XM_005246014.2:c.381+194G=	XP_005246071.1:n.381+194G=
XM_011542270.1:c.630+194G=	XP_011540572.1:n.630+194G=
XM_011542271.1:c.381+194G=	XP_011540573.1:n.381+194G=
XM_011542272.1:c.381+194G=	XP_011540574.1:n.381+194G=
XM_011542273.1:c.630+194G=	XP_011540575.1:n.630+194G=
XR_946778.1:n.795+194G=
XM_011542273.3:c.630+194G=	XP_011540575.1:n.630+194G=
NM_001229.5:c.630+194G= MANE Select	NP_001220.2:n.630+194G=
NM_001278054.2:c.419-11253G=	NP_001264983.1:n.419-11253G=
NR_102732.2:n.703+194G=
NR_102733.2:n.505+194G=