Canonical Allele Identifier: CA1821104972

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133644T= , CM000670.2:g.133133644T=	GRCh38
NC_000008.10:g.134145888T= , CM000670.1:g.134145888T=	GRCh37
NC_000008.9:g.134215070T=	NCBI36
NG_015832.1:g.271684T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8172T= MANE Select	ENSP00000220616.4:p.Ser2724=
ENST00000220616.8:c.8172T=	ENSP00000220616.4:p.Ser2724=
ENST00000519178.5:c.3538T=
ENST00000519543.5:c.2571T=	ENSP00000430430.1:p.Ser857=
ENST00000521107.1:c.384T=	ENSP00000430161.1:p.Ser128=
ENST00000522691.1:n.258T=
ENST00000523756.5:c.4827T=
NM_003235.4:c.8172T=	NP_003226.4:p.Ser2724=
XM_005251038.3:c.7980T=	XP_005251095.1:p.Ser2660=
XM_006716622.2:c.8109T=	XP_006716685.1:p.Ser2703=
XM_005251038.4:c.7980T=	XP_005251095.1:p.Ser2660=
XM_006716622.3:c.8109T=	XP_006716685.1:p.Ser2703=
XM_017013793.1:c.8106T=	XP_016869282.1:p.Ser2702=
XM_017013794.1:c.8037T=	XP_016869283.1:p.Ser2679=
XM_017013795.1:c.8001T=	XP_016869284.1:p.Ser2667=
XM_017013796.1:c.7953T=	XP_016869285.1:p.Ser2651=
XM_017013797.1:c.7911T=	XP_016869286.1:p.Ser2637=
NM_003235.5:c.8172T= MANE Select	NP_003226.4:p.Ser2724=