Canonical Allele Identifier: CA1821046461

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017988G= , CM000670.2:g.133017988G=	GRCh38
NC_000008.10:g.134030233G= , CM000670.1:g.134030233G=	GRCh37
NC_000008.9:g.134099415G=	NCBI36
NG_015832.1:g.156029G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6773G= MANE Select	ENSP00000220616.4:p.Ser2258=
ENST00000220616.8:c.6773G=	ENSP00000220616.4:p.Ser2258=
ENST00000518108.1:c.168+122G=
ENST00000519178.5:c.2139G=
ENST00000519543.5:c.1172G=	ENSP00000430430.1:p.Ser391=
ENST00000523756.5:c.3428G=
NM_003235.4:c.6773G=	NP_003226.4:p.Ser2258=
XM_005251038.3:c.6581G=	XP_005251095.1:p.Ser2194=
XM_006716622.2:c.6710G=	XP_006716685.1:p.Ser2237=
XM_005251038.4:c.6581G=	XP_005251095.1:p.Ser2194=
XM_006716622.3:c.6710G=	XP_006716685.1:p.Ser2237=
XM_017013793.1:c.6707G=	XP_016869282.1:p.Ser2236=
XM_017013794.1:c.6773G=	XP_016869283.1:p.Ser2258=
XM_017013795.1:c.6602G=	XP_016869284.1:p.Ser2201=
XM_017013796.1:c.6554G=	XP_016869285.1:p.Ser2185=
XM_017013797.1:c.6512G=	XP_016869286.1:p.Ser2171=
XM_017013798.1:c.6773G=	XP_016869287.1:p.Ser2258=
NM_003235.5:c.6773G= MANE Select	NP_003226.4:p.Ser2258=