Canonical Allele Identifier: CA372253609

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145874A>C (hg19) ; chr8:g.133133630A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133630A>C , CM000670.2:g.133133630A>C	GRCh38
NC_000008.10:g.134145874A>C , CM000670.1:g.134145874A>C	GRCh37
NC_000008.9:g.134215056A>C	NCBI36
NG_015832.1:g.271670A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8158A>C MANE Select	ENSP00000220616.4:p.Lys2720Gln
ENST00000220616.8:c.8158A>C	ENSP00000220616.4:p.Lys2720Gln
ENST00000519178.5:c.3524A>C
ENST00000519543.5:c.2557A>C	ENSP00000430430.1:p.Lys853Gln
ENST00000521107.1:c.370A>C	ENSP00000430161.1:p.Lys124Gln
ENST00000522691.1:n.244A>C
ENST00000523756.5:c.4813A>C
NM_003235.4:c.8158A>C	NP_003226.4:p.Lys2720Gln
XM_005251038.3:c.7966A>C	XP_005251095.1:p.Lys2656Gln
XM_006716622.2:c.8095A>C	XP_006716685.1:p.Lys2699Gln
XM_005251038.4:c.7966A>C	XP_005251095.1:p.Lys2656Gln
XM_006716622.3:c.8095A>C	XP_006716685.1:p.Lys2699Gln
XM_017013793.1:c.8092A>C	XP_016869282.1:p.Lys2698Gln
XM_017013794.1:c.8023A>C	XP_016869283.1:p.Lys2675Gln
XM_017013795.1:c.7987A>C	XP_016869284.1:p.Lys2663Gln
XM_017013796.1:c.7939A>C	XP_016869285.1:p.Lys2647Gln
XM_017013797.1:c.7897A>C	XP_016869286.1:p.Lys2633Gln
NM_003235.5:c.8158A>C MANE Select	NP_003226.4:p.Lys2720Gln