Canonical Allele Identifier: CA372253221

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145778T>A (hg19) ; chr8:g.133133534T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133534T>A , CM000670.2:g.133133534T>A	GRCh38
NC_000008.10:g.134145778T>A , CM000670.1:g.134145778T>A	GRCh37
NC_000008.9:g.134214960T>A	NCBI36
NG_015832.1:g.271574T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8062T>A MANE Select	ENSP00000220616.4:p.Phe2688Ile
ENST00000220616.8:c.8062T>A	ENSP00000220616.4:p.Phe2688Ile
ENST00000519178.5:c.3428T>A
ENST00000519543.5:c.2461T>A	ENSP00000430430.1:p.Phe821Ile
ENST00000521107.1:c.274T>A	ENSP00000430161.1:p.Phe92Ile
ENST00000522691.1:n.148T>A
ENST00000523756.5:c.4717T>A
NM_003235.4:c.8062T>A	NP_003226.4:p.Phe2688Ile
XM_005251038.3:c.7870T>A	XP_005251095.1:p.Phe2624Ile
XM_006716622.2:c.7999T>A	XP_006716685.1:p.Phe2667Ile
XM_005251038.4:c.7870T>A	XP_005251095.1:p.Phe2624Ile
XM_006716622.3:c.7999T>A	XP_006716685.1:p.Phe2667Ile
XM_017013793.1:c.7996T>A	XP_016869282.1:p.Phe2666Ile
XM_017013794.1:c.7927T>A	XP_016869283.1:p.Phe2643Ile
XM_017013795.1:c.7891T>A	XP_016869284.1:p.Phe2631Ile
XM_017013796.1:c.7843T>A	XP_016869285.1:p.Phe2615Ile
XM_017013797.1:c.7801T>A	XP_016869286.1:p.Phe2601Ile
NM_003235.5:c.8062T>A MANE Select	NP_003226.4:p.Phe2688Ile