Canonical Allele Identifier: CA372253695

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145896C>A (hg19) ; chr8:g.133133652C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133652C>A , CM000670.2:g.133133652C>A	GRCh38
NC_000008.10:g.134145896C>A , CM000670.1:g.134145896C>A	GRCh37
NC_000008.9:g.134215078C>A	NCBI36
NG_015832.1:g.271692C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8180C>A MANE Select	ENSP00000220616.4:p.Thr2727Lys
ENST00000220616.8:c.8180C>A	ENSP00000220616.4:p.Thr2727Lys
ENST00000519178.5:c.3546C>A
ENST00000519543.5:c.2579C>A	ENSP00000430430.1:p.Thr860Lys
ENST00000521107.1:c.392C>A	ENSP00000430161.1:p.Thr131Lys
ENST00000522691.1:n.266C>A
ENST00000523756.5:c.4835C>A
NM_003235.4:c.8180C>A	NP_003226.4:p.Thr2727Lys
XM_005251038.3:c.7988C>A	XP_005251095.1:p.Thr2663Lys
XM_006716622.2:c.8117C>A	XP_006716685.1:p.Thr2706Lys
XM_005251038.4:c.7988C>A	XP_005251095.1:p.Thr2663Lys
XM_006716622.3:c.8117C>A	XP_006716685.1:p.Thr2706Lys
XM_017013793.1:c.8114C>A	XP_016869282.1:p.Thr2705Lys
XM_017013794.1:c.8045C>A	XP_016869283.1:p.Thr2682Lys
XM_017013795.1:c.8009C>A	XP_016869284.1:p.Thr2670Lys
XM_017013796.1:c.7961C>A	XP_016869285.1:p.Thr2654Lys
XM_017013797.1:c.7919C>A	XP_016869286.1:p.Thr2640Lys
NM_003235.5:c.8180C>A MANE Select	NP_003226.4:p.Thr2727Lys