Canonical Allele Identifier: CA372253689

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145895A>C (hg19) ; chr8:g.133133651A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133651A>C , CM000670.2:g.133133651A>C	GRCh38
NC_000008.10:g.134145895A>C , CM000670.1:g.134145895A>C	GRCh37
NC_000008.9:g.134215077A>C	NCBI36
NG_015832.1:g.271691A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8179A>C MANE Select	ENSP00000220616.4:p.Thr2727Pro
ENST00000220616.8:c.8179A>C	ENSP00000220616.4:p.Thr2727Pro
ENST00000519178.5:c.3545A>C
ENST00000519543.5:c.2578A>C	ENSP00000430430.1:p.Thr860Pro
ENST00000521107.1:c.391A>C	ENSP00000430161.1:p.Thr131Pro
ENST00000522691.1:n.265A>C
ENST00000523756.5:c.4834A>C
NM_003235.4:c.8179A>C	NP_003226.4:p.Thr2727Pro
XM_005251038.3:c.7987A>C	XP_005251095.1:p.Thr2663Pro
XM_006716622.2:c.8116A>C	XP_006716685.1:p.Thr2706Pro
XM_005251038.4:c.7987A>C	XP_005251095.1:p.Thr2663Pro
XM_006716622.3:c.8116A>C	XP_006716685.1:p.Thr2706Pro
XM_017013793.1:c.8113A>C	XP_016869282.1:p.Thr2705Pro
XM_017013794.1:c.8044A>C	XP_016869283.1:p.Thr2682Pro
XM_017013795.1:c.8008A>C	XP_016869284.1:p.Thr2670Pro
XM_017013796.1:c.7960A>C	XP_016869285.1:p.Thr2654Pro
XM_017013797.1:c.7918A>C	XP_016869286.1:p.Thr2640Pro
NM_003235.5:c.8179A>C MANE Select	NP_003226.4:p.Thr2727Pro