Canonical Allele Identifier: CA1821104952

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133601T= , CM000670.2:g.133133601T=	GRCh38
NC_000008.10:g.134145845T= , CM000670.1:g.134145845T=	GRCh37
NC_000008.9:g.134215027T=	NCBI36
NG_015832.1:g.271641T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8129T= MANE Select	ENSP00000220616.4:p.Leu2710=
ENST00000220616.8:c.8129T=	ENSP00000220616.4:p.Leu2710=
ENST00000519178.5:c.3495T=
ENST00000519543.5:c.2528T=	ENSP00000430430.1:p.Leu843=
ENST00000521107.1:c.341T=	ENSP00000430161.1:p.Leu114=
ENST00000522691.1:n.215T=
ENST00000523756.5:c.4784T=
NM_003235.4:c.8129T=	NP_003226.4:p.Leu2710=
XM_005251038.3:c.7937T=	XP_005251095.1:p.Leu2646=
XM_006716622.2:c.8066T=	XP_006716685.1:p.Leu2689=
XM_005251038.4:c.7937T=	XP_005251095.1:p.Leu2646=
XM_006716622.3:c.8066T=	XP_006716685.1:p.Leu2689=
XM_017013793.1:c.8063T=	XP_016869282.1:p.Leu2688=
XM_017013794.1:c.7994T=	XP_016869283.1:p.Leu2665=
XM_017013795.1:c.7958T=	XP_016869284.1:p.Leu2653=
XM_017013796.1:c.7910T=	XP_016869285.1:p.Leu2637=
XM_017013797.1:c.7868T=	XP_016869286.1:p.Leu2623=
NM_003235.5:c.8129T= MANE Select	NP_003226.4:p.Leu2710=