Canonical Allele Identifier: CA463017180

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145825G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133581G>A , CM000670.2:g.133133581G>A	GRCh38
NC_000008.10:g.134145825G>A , CM000670.1:g.134145825G>A	GRCh37
NC_000008.9:g.134215007G>A	NCBI36
NG_015832.1:g.271621G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8109G>A MANE Select	ENSP00000220616.4:p.Leu2703=
ENST00000220616.8:c.8109G>A	ENSP00000220616.4:p.Leu2703=
ENST00000519178.5:c.3475G>A
ENST00000519543.5:c.2508G>A	ENSP00000430430.1:p.Leu836=
ENST00000521107.1:c.321G>A	ENSP00000430161.1:p.Leu107=
ENST00000522691.1:n.195G>A
ENST00000523756.5:c.4764G>A
NM_003235.4:c.8109G>A	NP_003226.4:p.Leu2703=
XM_005251038.3:c.7917G>A	XP_005251095.1:p.Leu2639=
XM_006716622.2:c.8046G>A	XP_006716685.1:p.Leu2682=
XM_005251038.4:c.7917G>A	XP_005251095.1:p.Leu2639=
XM_006716622.3:c.8046G>A	XP_006716685.1:p.Leu2682=
XM_017013793.1:c.8043G>A	XP_016869282.1:p.Leu2681=
XM_017013794.1:c.7974G>A	XP_016869283.1:p.Leu2658=
XM_017013795.1:c.7938G>A	XP_016869284.1:p.Leu2646=
XM_017013796.1:c.7890G>A	XP_016869285.1:p.Leu2630=
XM_017013797.1:c.7848G>A	XP_016869286.1:p.Leu2616=
NM_003235.5:c.8109G>A MANE Select	NP_003226.4:p.Leu2703=