Canonical Allele Identifier: CA15087853

Gene: CASP9

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15498700T>C , CM000663.2:g.15498700T>C	GRCh38
NC_000001.10:g.15825195T>C , CM000663.1:g.15825195T>C	GRCh37
NC_000001.9:g.15697782T>C	NCBI36
NG_029188.1:g.31091A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333868.10:c.869-3248A>G MANE Select	ENSP00000330237.5:n.869-3248A>G
ENST00000333868.9:c.869-3248A>G	ENSP00000330237.5:n.869-3248A>G
ENST00000348549.9:c.419-3248A>G	ENSP00000255256.7:n.419-3248A>G
ENST00000375890.8:c.620-3248A>G	ENSP00000365051.4:n.620-3248A>G
ENST00000400777.7:c.919-3248A>G
ENST00000424908.5:c.393-4699A>G
ENST00000447522.5:c.620-3248A>G	ENSP00000396540.1:n.620-3248A>G
ENST00000474305.2:c.729-3248A>G	ENSP00000449216.1:n.729-3248A>G
ENST00000546424.5:c.869-3248A>G	ENSP00000449584.1:n.869-3248A>G
NM_001229.4:c.869-3248A>G	NP_001220.2:n.869-3248A>G
NM_001278054.1:c.419-3248A>G	NP_001264983.1:n.419-3248A>G
NM_032996.3:c.620-3248A>G	NP_127463.2:n.620-3248A>G
NR_102732.1:n.1172-3248A>G
NR_102733.1:n.974-3248A>G
XM_005246014.2:c.620-3248A>G	XP_005246071.1:n.620-3248A>G
XM_011542271.1:c.620-3248A>G	XP_011540573.1:n.620-3248A>G
XM_011542272.1:c.620-3248A>G	XP_011540574.1:n.620-3248A>G
XM_011542273.1:c.869-3248A>G	XP_011540575.1:n.869-3248A>G
XR_946778.1:n.796-3248A>G
XM_011542273.3:c.869-3248A>G	XP_011540575.1:n.869-3248A>G
NM_001229.5:c.869-3248A>G MANE Select	NP_001220.2:n.869-3248A>G
NM_001278054.2:c.419-3248A>G	NP_001264983.1:n.419-3248A>G
NR_102732.2:n.942-3248A>G
NR_102733.2:n.744-3248A>G