Canonical Allele Identifier: CA273804771

Gene: IDH3A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78161655G>A , CM000677.2:g.78161655G>A	GRCh38
NC_000015.9:g.78453997G>A , CM000677.1:g.78453997G>A	GRCh37
NC_000015.8:g.76241052G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005530.3:c.364G>A MANE Select	NP_005521.1:p.Ala122Thr
ENST00000299518.7:c.364G>A MANE Select	ENSP00000299518.2:p.Ala122Thr
NM_005530.2:c.364G>A	NP_005521.1:p.Ala122Thr
ENST00000299518.6:c.364G>A	ENSP00000299518.2:p.Ala122Thr
ENST00000558509.5:c.*66G>A	ENSP00000453992.1:n.*66G>A
ENST00000558535.1:n.312G>A
ENST00000558554.5:c.290-31G>A	ENSP00000453084.1:n.290-31G>A
ENST00000558602.5:n.899G>A
ENST00000558933.5:c.*66G>A	ENSP00000452620.1:n.*66G>A
ENST00000559186.5:c.214G>A	ENSP00000452754.1:p.Ala72Thr
ENST00000559205.1:c.28-4495G>A	ENSP00000453989.1:n.28-4495G>A
ENST00000559803.5:c.*66G>A	ENSP00000453338.1:n.*66G>A
ENST00000559865.5:c.*390G>A	ENSP00000453438.1:n.*390G>A
ENST00000559881.5:c.214G>A	ENSP00000453222.1:p.Ala72Thr
ENST00000559889.5:n.1030G>A
ENST00000560396.5:c.*210G>A	ENSP00000453192.1:n.*210G>A
ENST00000560667.5:c.*505G>A	ENSP00000453033.1:n.*505G>A
ENST00000561279.5:c.280G>A	ENSP00000453747.1:p.Ala94Thr
XM_005254334.1:c.214G>A	XP_005254391.1:p.Ala72Thr
XM_005254336.1:c.37G>A	XP_005254393.1:p.Ala13Thr
XM_005254336.3:c.37G>A	XP_005254393.1:p.Ala13Thr
XM_005254337.1:c.37G>A	XP_005254394.1:p.Ala13Thr
XM_024449911.1:c.214G>A	XP_024305679.1:p.Ala72Thr
XM_024449912.1:c.37G>A	XP_024305680.1:p.Ala13Thr