Canonical Allele Identifier: CA393542793

Gene: IDH3A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78161754G>T , CM000677.2:g.78161754G>T	GRCh38
NC_000015.9:g.78454096G>T , CM000677.1:g.78454096G>T	GRCh37
NC_000015.8:g.76241151G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005530.3:c.463G>T MANE Select	NP_005521.1:p.Gly155Ter
ENST00000299518.7:c.463G>T MANE Select	ENSP00000299518.2:p.Gly155Ter
NM_005530.2:c.463G>T	NP_005521.1:p.Gly155Ter
ENST00000299518.6:c.463G>T	ENSP00000299518.2:p.Gly155Ter
ENST00000558509.5:c.*165G>T	ENSP00000453992.1:n.*165G>T
ENST00000558535.1:n.411G>T
ENST00000558554.5:c.358G>T	ENSP00000453084.1:p.Gly120Ter
ENST00000558602.5:n.998G>T
ENST00000558933.5:c.*165G>T	ENSP00000452620.1:n.*165G>T
ENST00000559186.5:c.313G>T	ENSP00000452754.1:p.Gly105Ter
ENST00000559205.1:c.28-4396G>T	ENSP00000453989.1:n.28-4396G>T
ENST00000559803.5:c.*165G>T	ENSP00000453338.1:n.*165G>T
ENST00000559881.5:c.313G>T	ENSP00000453222.1:p.Gly105Ter
ENST00000559889.5:n.1129G>T
ENST00000560396.5:c.*309G>T	ENSP00000453192.1:n.*309G>T
ENST00000560667.5:c.*604G>T	ENSP00000453033.1:n.*604G>T
ENST00000561279.5:c.379G>T	ENSP00000453747.1:p.Gly127Ter
XM_005254334.1:c.313G>T	XP_005254391.1:p.Gly105Ter
XM_005254336.1:c.136G>T	XP_005254393.1:p.Gly46Ter
XM_005254336.3:c.136G>T	XP_005254393.1:p.Gly46Ter
XM_005254337.1:c.136G>T	XP_005254394.1:p.Gly46Ter
XM_024449911.1:c.313G>T	XP_024305679.1:p.Gly105Ter
XM_024449912.1:c.136G>T	XP_024305680.1:p.Gly46Ter