Canonical Allele Identifier: CA372253565

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145865T>A (hg19) ; chr8:g.133133621T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133621T>A , CM000670.2:g.133133621T>A	GRCh38
NC_000008.10:g.134145865T>A , CM000670.1:g.134145865T>A	GRCh37
NC_000008.9:g.134215047T>A	NCBI36
NG_015832.1:g.271661T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8149T>A MANE Select	ENSP00000220616.4:p.Phe2717Ile
ENST00000220616.8:c.8149T>A	ENSP00000220616.4:p.Phe2717Ile
ENST00000519178.5:c.3515T>A
ENST00000519543.5:c.2548T>A	ENSP00000430430.1:p.Phe850Ile
ENST00000521107.1:c.361T>A	ENSP00000430161.1:p.Phe121Ile
ENST00000522691.1:n.235T>A
ENST00000523756.5:c.4804T>A
NM_003235.4:c.8149T>A	NP_003226.4:p.Phe2717Ile
XM_005251038.3:c.7957T>A	XP_005251095.1:p.Phe2653Ile
XM_006716622.2:c.8086T>A	XP_006716685.1:p.Phe2696Ile
XM_005251038.4:c.7957T>A	XP_005251095.1:p.Phe2653Ile
XM_006716622.3:c.8086T>A	XP_006716685.1:p.Phe2696Ile
XM_017013793.1:c.8083T>A	XP_016869282.1:p.Phe2695Ile
XM_017013794.1:c.8014T>A	XP_016869283.1:p.Phe2672Ile
XM_017013795.1:c.7978T>A	XP_016869284.1:p.Phe2660Ile
XM_017013796.1:c.7930T>A	XP_016869285.1:p.Phe2644Ile
XM_017013797.1:c.7888T>A	XP_016869286.1:p.Phe2630Ile
NM_003235.5:c.8149T>A MANE Select	NP_003226.4:p.Phe2717Ile