Canonical Allele Identifier: CA372233714

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017940G>T , CM000670.2:g.133017940G>T	GRCh38
NC_000008.10:g.134030185G>T , CM000670.1:g.134030185G>T	GRCh37
NC_000008.9:g.134099367G>T	NCBI36
NG_015832.1:g.155981G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003235.5:c.6725G>T MANE Select	NP_003226.4:p.Arg2242Leu
ENST00000220616.9:c.6725G>T MANE Select	ENSP00000220616.4:p.Arg2242Leu
NM_003235.4:c.6725G>T	NP_003226.4:p.Arg2242Leu
ENST00000220616.8:c.6725G>T	ENSP00000220616.4:p.Arg2242Leu
ENST00000518108.1:c.168+74G>T
ENST00000519178.5:c.2091G>T
ENST00000519543.5:c.1124G>T	ENSP00000430430.1:p.Arg375Leu
ENST00000522523.5:n.786G>T
ENST00000523756.5:c.3380G>T
XM_005251038.3:c.6533G>T	XP_005251095.1:p.Arg2178Leu
XM_005251038.4:c.6533G>T	XP_005251095.1:p.Arg2178Leu
XM_006716622.2:c.6662G>T	XP_006716685.1:p.Arg2221Leu
XM_006716622.3:c.6662G>T	XP_006716685.1:p.Arg2221Leu
XM_017013793.1:c.6659G>T	XP_016869282.1:p.Arg2220Leu
XM_017013794.1:c.6725G>T	XP_016869283.1:p.Arg2242Leu
XM_017013795.1:c.6554G>T	XP_016869284.1:p.Arg2185Leu
XM_017013796.1:c.6506G>T	XP_016869285.1:p.Arg2169Leu
XM_017013797.1:c.6464G>T	XP_016869286.1:p.Arg2155Leu
XM_017013798.1:c.6725G>T	XP_016869287.1:p.Arg2242Leu