Canonical Allele Identifier: CA1155404927

Gene: CASP9

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.15507878_15507879delinsCT , CM000663.2:g.15507878_15507879delinsCT	GRCh38
NC_000001.10:g.15834373_15834374delinsCT , CM000663.1:g.15834373_15834374delinsCT	GRCh37
NC_000001.9:g.15706960_15706961delinsCT	NCBI36
NG_029188.1:g.21912_21913delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000333868.10:c.447_448delinsAG MANE Select	ENSP00000330237.5:p.Ala149=
ENST00000333868.9:c.447_448delinsAG	ENSP00000330237.5:p.Ala149=
ENST00000348549.9:c.418+10231_418+10232delinsAG	ENSP00000255256.7:n.418+10231_418+10232de...
ENST00000375890.8:c.198_199delinsAG	ENSP00000365051.4:p.Ala66=
ENST00000400777.7:c.439_440delinsAG
ENST00000440484.1:c.447_448delinsAG	ENSP00000411304.1:p.Ala149=
ENST00000447522.5:c.198_199delinsAG	ENSP00000396540.1:p.Ala66=
ENST00000474305.2:c.307_308delinsAG	ENSP00000449216.1:n.307_308delinsAG
ENST00000546424.5:c.447_448delinsAG	ENSP00000449584.1:p.Ala149=
ENST00000546969.1:n.462_463delinsAG
NM_001229.4:c.447_448delinsAG	NP_001220.2:p.Ala149=
NM_001278054.1:c.418+10231_418+10232delinsAG	NP_001264983.1:n.418+10231_418+10232delin...
NM_032996.3:c.198_199delinsAG	NP_127463.2:p.Ala66=
NR_102732.1:n.692_693delinsAG
NR_102733.1:n.552_553delinsAG
XM_005246014.2:c.198_199delinsAG	XP_005246071.1:p.Ala66=
XM_011542270.1:c.447_448delinsAG	XP_011540572.1:p.Ala149=
XM_011542271.1:c.198_199delinsAG	XP_011540573.1:p.Ala66=
XM_011542272.1:c.198_199delinsAG	XP_011540574.1:p.Ala66=
XM_011542273.1:c.447_448delinsAG	XP_011540575.1:p.Ala149=
XR_946778.1:n.612_613delinsAG
XM_011542273.3:c.447_448delinsAG	XP_011540575.1:p.Ala149=
NM_001229.5:c.447_448delinsAG MANE Select	NP_001220.2:p.Ala149=
NM_001278054.2:c.418+10231_418+10232delinsAG	NP_001264983.1:n.418+10231_418+10232delin...
NR_102732.2:n.462_463delinsAG
NR_102733.2:n.322_323delinsAG