Canonical Allele Identifier: CA1821104939

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133573A= , CM000670.2:g.133133573A=	GRCh38
NC_000008.10:g.134145817A= , CM000670.1:g.134145817A=	GRCh37
NC_000008.9:g.134214999A=	NCBI36
NG_015832.1:g.271613A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8101A= MANE Select	ENSP00000220616.4:p.Ser2701=
ENST00000220616.8:c.8101A=	ENSP00000220616.4:p.Ser2701=
ENST00000519178.5:c.3467A=
ENST00000519543.5:c.2500A=	ENSP00000430430.1:p.Ser834=
ENST00000521107.1:c.313A=	ENSP00000430161.1:p.Ser105=
ENST00000522691.1:n.187A=
ENST00000523756.5:c.4756A=
NM_003235.4:c.8101A=	NP_003226.4:p.Ser2701=
XM_005251038.3:c.7909A=	XP_005251095.1:p.Ser2637=
XM_006716622.2:c.8038A=	XP_006716685.1:p.Ser2680=
XM_005251038.4:c.7909A=	XP_005251095.1:p.Ser2637=
XM_006716622.3:c.8038A=	XP_006716685.1:p.Ser2680=
XM_017013793.1:c.8035A=	XP_016869282.1:p.Ser2679=
XM_017013794.1:c.7966A=	XP_016869283.1:p.Ser2656=
XM_017013795.1:c.7930A=	XP_016869284.1:p.Ser2644=
XM_017013796.1:c.7882A=	XP_016869285.1:p.Ser2628=
XM_017013797.1:c.7840A=	XP_016869286.1:p.Ser2614=
NM_003235.5:c.8101A= MANE Select	NP_003226.4:p.Ser2701=