Canonical Allele Identifier: CA372253090

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145745A>T (hg19) ; chr8:g.133133501A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133501A>T , CM000670.2:g.133133501A>T	GRCh38
NC_000008.10:g.134145745A>T , CM000670.1:g.134145745A>T	GRCh37
NC_000008.9:g.134214927A>T	NCBI36
NG_015832.1:g.271541A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8029A>T MANE Select	ENSP00000220616.4:p.Lys2677Ter
ENST00000220616.8:c.8029A>T	ENSP00000220616.4:p.Lys2677Ter
ENST00000519178.5:c.3395A>T
ENST00000519543.5:c.2428A>T	ENSP00000430430.1:p.Lys810Ter
ENST00000521107.1:c.241A>T	ENSP00000430161.1:p.Lys81Ter
ENST00000522691.1:n.115A>T
ENST00000523756.5:c.4684A>T
NM_003235.4:c.8029A>T	NP_003226.4:p.Lys2677Ter
XM_005251038.3:c.7837A>T	XP_005251095.1:p.Lys2613Ter
XM_006716622.2:c.7966A>T	XP_006716685.1:p.Lys2656Ter
XM_005251038.4:c.7837A>T	XP_005251095.1:p.Lys2613Ter
XM_006716622.3:c.7966A>T	XP_006716685.1:p.Lys2656Ter
XM_017013793.1:c.7963A>T	XP_016869282.1:p.Lys2655Ter
XM_017013794.1:c.7894A>T	XP_016869283.1:p.Lys2632Ter
XM_017013795.1:c.7858A>T	XP_016869284.1:p.Lys2620Ter
XM_017013796.1:c.7810A>T	XP_016869285.1:p.Lys2604Ter
XM_017013797.1:c.7768A>T	XP_016869286.1:p.Lys2590Ter
NM_003235.5:c.8029A>T MANE Select	NP_003226.4:p.Lys2677Ter