Canonical Allele Identifier: CA210709

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133029907G>A , CM000670.2:g.133029907G>A	GRCh38
NC_000008.10:g.134042152G>A , CM000670.1:g.134042152G>A	GRCh37
NC_000008.9:g.134111334G>A	NCBI36
NG_015832.1:g.167948G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003235.5:c.7123G>A MANE Select	NP_003226.4:p.Gly2375Arg
ENST00000220616.9:c.7123G>A MANE Select	ENSP00000220616.4:p.Gly2375Arg
NM_003235.4:c.7123G>A	NP_003226.4:p.Gly2375Arg
ENST00000220616.8:c.7123G>A	ENSP00000220616.4:p.Gly2375Arg
ENST00000518108.1:c.509G>A
ENST00000519178.5:c.2489G>A
ENST00000519543.5:c.1522G>A	ENSP00000430430.1:p.Gly508Arg
ENST00000523756.5:c.3778G>A
XM_005251038.3:c.6931G>A	XP_005251095.1:p.Gly2311Arg
XM_005251038.4:c.6931G>A	XP_005251095.1:p.Gly2311Arg
XM_006716622.2:c.7060G>A	XP_006716685.1:p.Gly2354Arg
XM_006716622.3:c.7060G>A	XP_006716685.1:p.Gly2354Arg
XM_017013793.1:c.7057G>A	XP_016869282.1:p.Gly2353Arg
XM_017013794.1:c.7123G>A	XP_016869283.1:p.Gly2375Arg
XM_017013795.1:c.6952G>A	XP_016869284.1:p.Gly2318Arg
XM_017013796.1:c.6904G>A	XP_016869285.1:p.Gly2302Arg
XM_017013797.1:c.6862G>A	XP_016869286.1:p.Gly2288Arg
XM_017013798.1:c.7123G>A	XP_016869287.1:p.Gly2375Arg