Canonical Allele Identifier: CA372253241

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145782T>A (hg19) ; chr8:g.133133538T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133538T>A , CM000670.2:g.133133538T>A	GRCh38
NC_000008.10:g.134145782T>A , CM000670.1:g.134145782T>A	GRCh37
NC_000008.9:g.134214964T>A	NCBI36
NG_015832.1:g.271578T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8066T>A MANE Select	ENSP00000220616.4:p.Val2689Glu
ENST00000220616.8:c.8066T>A	ENSP00000220616.4:p.Val2689Glu
ENST00000519178.5:c.3432T>A
ENST00000519543.5:c.2465T>A	ENSP00000430430.1:p.Val822Glu
ENST00000521107.1:c.278T>A	ENSP00000430161.1:p.Val93Glu
ENST00000522691.1:n.152T>A
ENST00000523756.5:c.4721T>A
NM_003235.4:c.8066T>A	NP_003226.4:p.Val2689Glu
XM_005251038.3:c.7874T>A	XP_005251095.1:p.Val2625Glu
XM_006716622.2:c.8003T>A	XP_006716685.1:p.Val2668Glu
XM_005251038.4:c.7874T>A	XP_005251095.1:p.Val2625Glu
XM_006716622.3:c.8003T>A	XP_006716685.1:p.Val2668Glu
XM_017013793.1:c.8000T>A	XP_016869282.1:p.Val2667Glu
XM_017013794.1:c.7931T>A	XP_016869283.1:p.Val2644Glu
XM_017013795.1:c.7895T>A	XP_016869284.1:p.Val2632Glu
XM_017013796.1:c.7847T>A	XP_016869285.1:p.Val2616Glu
XM_017013797.1:c.7805T>A	XP_016869286.1:p.Val2602Glu
NM_003235.5:c.8066T>A MANE Select	NP_003226.4:p.Val2689Glu