Canonical Allele Identifier: CA372253265

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145790G>A (hg19) ; chr8:g.133133546G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133546G>A , CM000670.2:g.133133546G>A	GRCh38
NC_000008.10:g.134145790G>A , CM000670.1:g.134145790G>A	GRCh37
NC_000008.9:g.134214972G>A	NCBI36
NG_015832.1:g.271586G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8074G>A MANE Select	ENSP00000220616.4:p.Ala2692Thr
ENST00000220616.8:c.8074G>A	ENSP00000220616.4:p.Ala2692Thr
ENST00000519178.5:c.3440G>A
ENST00000519543.5:c.2473G>A	ENSP00000430430.1:p.Ala825Thr
ENST00000521107.1:c.286G>A	ENSP00000430161.1:p.Ala96Thr
ENST00000522691.1:n.160G>A
ENST00000523756.5:c.4729G>A
NM_003235.4:c.8074G>A	NP_003226.4:p.Ala2692Thr
XM_005251038.3:c.7882G>A	XP_005251095.1:p.Ala2628Thr
XM_006716622.2:c.8011G>A	XP_006716685.1:p.Ala2671Thr
XM_005251038.4:c.7882G>A	XP_005251095.1:p.Ala2628Thr
XM_006716622.3:c.8011G>A	XP_006716685.1:p.Ala2671Thr
XM_017013793.1:c.8008G>A	XP_016869282.1:p.Ala2670Thr
XM_017013794.1:c.7939G>A	XP_016869283.1:p.Ala2647Thr
XM_017013795.1:c.7903G>A	XP_016869284.1:p.Ala2635Thr
XM_017013796.1:c.7855G>A	XP_016869285.1:p.Ala2619Thr
XM_017013797.1:c.7813G>A	XP_016869286.1:p.Ala2605Thr
NM_003235.5:c.8074G>A MANE Select	NP_003226.4:p.Ala2692Thr