Canonical Allele Identifier: CA372253046

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145733G>A (hg19) ; chr8:g.133133489G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133489G>A , CM000670.2:g.133133489G>A	GRCh38
NC_000008.10:g.134145733G>A , CM000670.1:g.134145733G>A	GRCh37
NC_000008.9:g.134214915G>A	NCBI36
NG_015832.1:g.271529G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8017G>A MANE Select	ENSP00000220616.4:p.Glu2673Lys
ENST00000220616.8:c.8017G>A	ENSP00000220616.4:p.Glu2673Lys
ENST00000519178.5:c.3383G>A
ENST00000519543.5:c.2416G>A	ENSP00000430430.1:p.Glu806Lys
ENST00000521107.1:c.229G>A	ENSP00000430161.1:p.Glu77Lys
ENST00000522691.1:n.103G>A
ENST00000523756.5:c.4672G>A
NM_003235.4:c.8017G>A	NP_003226.4:p.Glu2673Lys
XM_005251038.3:c.7825G>A	XP_005251095.1:p.Glu2609Lys
XM_006716622.2:c.7954G>A	XP_006716685.1:p.Glu2652Lys
XM_005251038.4:c.7825G>A	XP_005251095.1:p.Glu2609Lys
XM_006716622.3:c.7954G>A	XP_006716685.1:p.Glu2652Lys
XM_017013793.1:c.7951G>A	XP_016869282.1:p.Glu2651Lys
XM_017013794.1:c.7882G>A	XP_016869283.1:p.Glu2628Lys
XM_017013795.1:c.7846G>A	XP_016869284.1:p.Glu2616Lys
XM_017013796.1:c.7798G>A	XP_016869285.1:p.Glu2600Lys
XM_017013797.1:c.7756G>A	XP_016869286.1:p.Glu2586Lys
NM_003235.5:c.8017G>A MANE Select	NP_003226.4:p.Glu2673Lys