Canonical Allele Identifier: CA393544829

Gene: IDH3A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.78163507G>A , CM000677.2:g.78163507G>A	GRCh38
NC_000015.9:g.78455849G>A , CM000677.1:g.78455849G>A	GRCh37
NC_000015.8:g.76242904G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_005530.3:c.612G>A MANE Select	NP_005521.1:p.Met204Ile
ENST00000299518.7:c.612G>A MANE Select	ENSP00000299518.2:p.Met204Ile
NM_005530.2:c.612G>A	NP_005521.1:p.Met204Ile
ENST00000299518.6:c.612G>A	ENSP00000299518.2:p.Met204Ile
ENST00000558509.5:c.*351G>A	ENSP00000453992.1:n.*351G>A
ENST00000558535.1:n.560G>A
ENST00000558554.5:c.507G>A	ENSP00000453084.1:p.Met169Ile
ENST00000558602.5:n.1147G>A
ENST00000558933.5:c.*314G>A	ENSP00000452620.1:n.*314G>A
ENST00000559205.1:c.28-2643G>A	ENSP00000453989.1:n.28-2643G>A
ENST00000559803.5:c.*351G>A	ENSP00000453338.1:n.*351G>A
ENST00000559889.5:n.1303G>A
ENST00000560667.5:c.*753G>A	ENSP00000453033.1:n.*753G>A
XM_005254334.1:c.462G>A	XP_005254391.1:p.Met154Ile
XM_005254336.1:c.285G>A	XP_005254393.1:p.Met95Ile
XM_005254336.3:c.285G>A	XP_005254393.1:p.Met95Ile
XM_005254337.1:c.285G>A	XP_005254394.1:p.Met95Ile
XM_024449911.1:c.462G>A	XP_024305679.1:p.Met154Ile
XM_024449912.1:c.285G>A	XP_024305680.1:p.Met95Ile