Canonical Allele Identifier: CA338566453

Gene: CASP9

Linked Data

• MyVariant Identifiers: chr1:g.15832547C>T (hg19) ; chr1:g.15506052C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15506052C>T , CM000663.2:g.15506052C>T	GRCh38
NC_000001.10:g.15832547C>T , CM000663.1:g.15832547C>T	GRCh37
NC_000001.9:g.15705134C>T	NCBI36
NG_029188.1:g.23739G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000333868.10:c.658G>A MANE Select	ENSP00000330237.5:p.Ala220Thr
ENST00000333868.9:c.658G>A	ENSP00000330237.5:p.Ala220Thr
ENST00000348549.9:c.419-10600G>A	ENSP00000255256.7:n.419-10600G>A
ENST00000375890.8:c.409G>A	ENSP00000365051.4:p.Ala137Thr
ENST00000400777.7:c.708G>A
ENST00000424908.5:c.182G>A
ENST00000440484.1:c.630+847G>A	ENSP00000411304.1:n.630+847G>A
ENST00000447522.5:c.409G>A	ENSP00000396540.1:p.Ala137Thr
ENST00000474305.2:c.518G>A	ENSP00000449216.1:n.518G>A
ENST00000546424.5:c.658G>A	ENSP00000449584.1:p.Ala220Thr
NM_001229.4:c.658G>A	NP_001220.2:p.Ala220Thr
NM_001278054.1:c.419-10600G>A	NP_001264983.1:n.419-10600G>A
NM_032996.3:c.409G>A	NP_127463.2:p.Ala137Thr
NR_102732.1:n.961G>A
NR_102733.1:n.763G>A
XM_005246014.2:c.409G>A	XP_005246071.1:p.Ala137Thr
XM_011542270.1:c.658G>A	XP_011540572.1:p.Ala220Thr
XM_011542271.1:c.409G>A	XP_011540573.1:p.Ala137Thr
XM_011542272.1:c.409G>A	XP_011540574.1:p.Ala137Thr
XM_011542273.1:c.658G>A	XP_011540575.1:p.Ala220Thr
XR_946778.1:n.795+847G>A
XM_011542273.3:c.658G>A	XP_011540575.1:p.Ala220Thr
NM_001229.5:c.658G>A MANE Select	NP_001220.2:p.Ala220Thr
NM_001278054.2:c.419-10600G>A	NP_001264983.1:n.419-10600G>A
NR_102732.2:n.731G>A
NR_102733.2:n.533G>A