Canonical Allele Identifier: CA372253533

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145857A>T (hg19) ; chr8:g.133133613A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133613A>T , CM000670.2:g.133133613A>T	GRCh38
NC_000008.10:g.134145857A>T , CM000670.1:g.134145857A>T	GRCh37
NC_000008.9:g.134215039A>T	NCBI36
NG_015832.1:g.271653A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8141A>T MANE Select	ENSP00000220616.4:p.Asp2714Val
ENST00000220616.8:c.8141A>T	ENSP00000220616.4:p.Asp2714Val
ENST00000519178.5:c.3507A>T
ENST00000519543.5:c.2540A>T	ENSP00000430430.1:p.Asp847Val
ENST00000521107.1:c.353A>T	ENSP00000430161.1:p.Asp118Val
ENST00000522691.1:n.227A>T
ENST00000523756.5:c.4796A>T
NM_003235.4:c.8141A>T	NP_003226.4:p.Asp2714Val
XM_005251038.3:c.7949A>T	XP_005251095.1:p.Asp2650Val
XM_006716622.2:c.8078A>T	XP_006716685.1:p.Asp2693Val
XM_005251038.4:c.7949A>T	XP_005251095.1:p.Asp2650Val
XM_006716622.3:c.8078A>T	XP_006716685.1:p.Asp2693Val
XM_017013793.1:c.8075A>T	XP_016869282.1:p.Asp2692Val
XM_017013794.1:c.8006A>T	XP_016869283.1:p.Asp2669Val
XM_017013795.1:c.7970A>T	XP_016869284.1:p.Asp2657Val
XM_017013796.1:c.7922A>T	XP_016869285.1:p.Asp2641Val
XM_017013797.1:c.7880A>T	XP_016869286.1:p.Asp2627Val
NM_003235.5:c.8141A>T MANE Select	NP_003226.4:p.Asp2714Val