Canonical Allele Identifier: CA1821104953

Gene: TG

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133602G= , CM000670.2:g.133133602G=	GRCh38
NC_000008.10:g.134145846G= , CM000670.1:g.134145846G=	GRCh37
NC_000008.9:g.134215028G=	NCBI36
NG_015832.1:g.271642G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8130G= MANE Select	ENSP00000220616.4:p.Leu2710=
ENST00000220616.8:c.8130G=	ENSP00000220616.4:p.Leu2710=
ENST00000519178.5:c.3496G=
ENST00000519543.5:c.2529G=	ENSP00000430430.1:p.Leu843=
ENST00000521107.1:c.342G=	ENSP00000430161.1:p.Leu114=
ENST00000522691.1:n.216G=
ENST00000523756.5:c.4785G=
NM_003235.4:c.8130G=	NP_003226.4:p.Leu2710=
XM_005251038.3:c.7938G=	XP_005251095.1:p.Leu2646=
XM_006716622.2:c.8067G=	XP_006716685.1:p.Leu2689=
XM_005251038.4:c.7938G=	XP_005251095.1:p.Leu2646=
XM_006716622.3:c.8067G=	XP_006716685.1:p.Leu2689=
XM_017013793.1:c.8064G=	XP_016869282.1:p.Leu2688=
XM_017013794.1:c.7995G=	XP_016869283.1:p.Leu2665=
XM_017013795.1:c.7959G=	XP_016869284.1:p.Leu2653=
XM_017013796.1:c.7911G=	XP_016869285.1:p.Leu2637=
XM_017013797.1:c.7869G=	XP_016869286.1:p.Leu2623=
NM_003235.5:c.8130G= MANE Select	NP_003226.4:p.Leu2710=