Canonical Allele Identifier: CA416177796

Gene: CASP9

Linked Data

• MyVariant Identifiers: chr1:g.15834374T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15507879T>C , CM000663.2:g.15507879T>C	GRCh38
NC_000001.10:g.15834374T>C , CM000663.1:g.15834374T>C	GRCh37
NC_000001.9:g.15706961T>C	NCBI36
NG_029188.1:g.21912A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000333868.10:c.447A>G MANE Select	ENSP00000330237.5:p.Ala149=
ENST00000333868.9:c.447A>G	ENSP00000330237.5:p.Ala149=
ENST00000348549.9:c.418+10231A>G	ENSP00000255256.7:n.418+10231A>G
ENST00000375890.8:c.198A>G	ENSP00000365051.4:p.Ala66=
ENST00000400777.7:c.439A>G
ENST00000440484.1:c.447A>G	ENSP00000411304.1:p.Ala149=
ENST00000447522.5:c.198A>G	ENSP00000396540.1:p.Ala66=
ENST00000474305.2:c.307A>G	ENSP00000449216.1:n.307A>G
ENST00000546424.5:c.447A>G	ENSP00000449584.1:p.Ala149=
ENST00000546969.1:n.462A>G
NM_001229.4:c.447A>G	NP_001220.2:p.Ala149=
NM_001278054.1:c.418+10231A>G	NP_001264983.1:n.418+10231A>G
NM_032996.3:c.198A>G	NP_127463.2:p.Ala66=
NR_102732.1:n.692A>G
NR_102733.1:n.552A>G
XM_005246014.2:c.198A>G	XP_005246071.1:p.Ala66=
XM_011542270.1:c.447A>G	XP_011540572.1:p.Ala149=
XM_011542271.1:c.198A>G	XP_011540573.1:p.Ala66=
XM_011542272.1:c.198A>G	XP_011540574.1:p.Ala66=
XM_011542273.1:c.447A>G	XP_011540575.1:p.Ala149=
XR_946778.1:n.612A>G
XM_011542273.3:c.447A>G	XP_011540575.1:p.Ala149=
NM_001229.5:c.447A>G MANE Select	NP_001220.2:p.Ala149=
NM_001278054.2:c.418+10231A>G	NP_001264983.1:n.418+10231A>G
NR_102732.2:n.462A>G
NR_102733.2:n.322A>G