Canonical Allele Identifier: CA614453

Gene: CASP9

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15504656G>T , CM000663.2:g.15504656G>T	GRCh38
NC_000001.10:g.15831151G>T , CM000663.1:g.15831151G>T	GRCh37
NC_000001.9:g.15703738G>T	NCBI36
NG_029188.1:g.25135C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000333868.10:c.823C>A MANE Select	ENSP00000330237.5:p.Leu275Met
ENST00000333868.9:c.823C>A	ENSP00000330237.5:p.Leu275Met
ENST00000348549.9:c.419-9204C>A	ENSP00000255256.7:n.419-9204C>A
ENST00000375890.8:c.574C>A	ENSP00000365051.4:p.Leu192Met
ENST00000400777.7:c.873C>A
ENST00000424908.5:c.347C>A
ENST00000440484.1:c.733C>A	ENSP00000411304.1:p.Leu245Met
ENST00000447522.5:c.574C>A	ENSP00000396540.1:p.Leu192Met
ENST00000474305.2:c.683C>A	ENSP00000449216.1:n.683C>A
ENST00000546424.5:c.823C>A	ENSP00000449584.1:p.Leu275Met
NM_001229.4:c.823C>A	NP_001220.2:p.Leu275Met
NM_001278054.1:c.419-9204C>A	NP_001264983.1:n.419-9204C>A
NM_032996.3:c.574C>A	NP_127463.2:p.Leu192Met
NR_102732.1:n.1126C>A
NR_102733.1:n.928C>A
XM_005246014.2:c.574C>A	XP_005246071.1:p.Leu192Met
XM_011542270.1:c.823C>A	XP_011540572.1:p.Leu275Met
XM_011542271.1:c.574C>A	XP_011540573.1:p.Leu192Met
XM_011542272.1:c.574C>A	XP_011540574.1:p.Leu192Met
XM_011542273.1:c.823C>A	XP_011540575.1:p.Leu275Met
XR_946778.1:n.795+2243C>A
XM_011542273.3:c.823C>A	XP_011540575.1:p.Leu275Met
NM_001229.5:c.823C>A MANE Select	NP_001220.2:p.Leu275Met
NM_001278054.2:c.419-9204C>A	NP_001264983.1:n.419-9204C>A
NR_102732.2:n.896C>A
NR_102733.2:n.698C>A