Canonical Allele Identifier: CA372253490

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145847A>G (hg19) ; chr8:g.133133603A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133603A>G , CM000670.2:g.133133603A>G	GRCh38
NC_000008.10:g.134145847A>G , CM000670.1:g.134145847A>G	GRCh37
NC_000008.9:g.134215029A>G	NCBI36
NG_015832.1:g.271643A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8131A>G MANE Select	ENSP00000220616.4:p.Lys2711Glu
ENST00000220616.8:c.8131A>G	ENSP00000220616.4:p.Lys2711Glu
ENST00000519178.5:c.3497A>G
ENST00000519543.5:c.2530A>G	ENSP00000430430.1:p.Lys844Glu
ENST00000521107.1:c.343A>G	ENSP00000430161.1:p.Lys115Glu
ENST00000522691.1:n.217A>G
ENST00000523756.5:c.4786A>G
NM_003235.4:c.8131A>G	NP_003226.4:p.Lys2711Glu
XM_005251038.3:c.7939A>G	XP_005251095.1:p.Lys2647Glu
XM_006716622.2:c.8068A>G	XP_006716685.1:p.Lys2690Glu
XM_005251038.4:c.7939A>G	XP_005251095.1:p.Lys2647Glu
XM_006716622.3:c.8068A>G	XP_006716685.1:p.Lys2690Glu
XM_017013793.1:c.8065A>G	XP_016869282.1:p.Lys2689Glu
XM_017013794.1:c.7996A>G	XP_016869283.1:p.Lys2666Glu
XM_017013795.1:c.7960A>G	XP_016869284.1:p.Lys2654Glu
XM_017013796.1:c.7912A>G	XP_016869285.1:p.Lys2638Glu
XM_017013797.1:c.7870A>G	XP_016869286.1:p.Lys2624Glu
NM_003235.5:c.8131A>G MANE Select	NP_003226.4:p.Lys2711Glu