Canonical Allele Identifier: CA372253281
Gene: TG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133133550G>A , CM000670.2:g.133133550G>A GRCh38
NC_000008.10:g.134145794G>A , CM000670.1:g.134145794G>A GRCh37
NC_000008.9:g.134214976G>A NCBI36
NG_015832.1:g.271590G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.8078G>A MANE Select ENSP00000220616.4:p.Gly2693Asp
ENST00000220616.8:c.8078G>A ENSP00000220616.4:p.Gly2693Asp
ENST00000519178.5:c.3444G>A
ENST00000519543.5:c.2477G>A ENSP00000430430.1:p.Gly826Asp
ENST00000521107.1:c.290G>A ENSP00000430161.1:p.Gly97Asp
ENST00000522691.1:n.164G>A
ENST00000523756.5:c.4733G>A
NM_003235.4:c.8078G>A NP_003226.4:p.Gly2693Asp
XM_005251038.3:c.7886G>A XP_005251095.1:p.Gly2629Asp
XM_006716622.2:c.8015G>A XP_006716685.1:p.Gly2672Asp
XM_005251038.4:c.7886G>A XP_005251095.1:p.Gly2629Asp
XM_006716622.3:c.8015G>A XP_006716685.1:p.Gly2672Asp
XM_017013793.1:c.8012G>A XP_016869282.1:p.Gly2671Asp
XM_017013794.1:c.7943G>A XP_016869283.1:p.Gly2648Asp
XM_017013795.1:c.7907G>A XP_016869284.1:p.Gly2636Asp
XM_017013796.1:c.7859G>A XP_016869285.1:p.Gly2620Asp
XM_017013797.1:c.7817G>A XP_016869286.1:p.Gly2606Asp
NM_003235.5:c.8078G>A MANE Select NP_003226.4:p.Gly2693Asp