Canonical Allele Identifier: CA1155401182

Gene: CASP9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15506059C= , CM000663.2:g.15506059C=	GRCh38
NC_000001.10:g.15832554C= , CM000663.1:g.15832554C=	GRCh37
NC_000001.9:g.15705141C=	NCBI36
NG_029188.1:g.23732G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000333868.10:c.651G= MANE Select	ENSP00000330237.5:p.Leu217=
ENST00000333868.9:c.651G=	ENSP00000330237.5:p.Leu217=
ENST00000348549.9:c.419-10607G=	ENSP00000255256.7:n.419-10607G=
ENST00000375890.8:c.402G=	ENSP00000365051.4:p.Leu134=
ENST00000400777.7:c.701G=
ENST00000424908.5:c.175G=
ENST00000440484.1:c.630+840G=	ENSP00000411304.1:n.630+840G=
ENST00000447522.5:c.402G=	ENSP00000396540.1:p.Leu134=
ENST00000474305.2:c.511G=	ENSP00000449216.1:n.511G=
ENST00000546424.5:c.651G=	ENSP00000449584.1:p.Leu217=
NM_001229.4:c.651G=	NP_001220.2:p.Leu217=
NM_001278054.1:c.419-10607G=	NP_001264983.1:n.419-10607G=
NM_032996.3:c.402G=	NP_127463.2:p.Leu134=
NR_102732.1:n.954G=
NR_102733.1:n.756G=
XM_005246014.2:c.402G=	XP_005246071.1:p.Leu134=
XM_011542270.1:c.651G=	XP_011540572.1:p.Leu217=
XM_011542271.1:c.402G=	XP_011540573.1:p.Leu134=
XM_011542272.1:c.402G=	XP_011540574.1:p.Leu134=
XM_011542273.1:c.651G=	XP_011540575.1:p.Leu217=
XR_946778.1:n.795+840G=
XM_011542273.3:c.651G=	XP_011540575.1:p.Leu217=
NM_001229.5:c.651G= MANE Select	NP_001220.2:p.Leu217=
NM_001278054.2:c.419-10607G=	NP_001264983.1:n.419-10607G=
NR_102732.2:n.724G=
NR_102733.2:n.526G=