Canonical Allele Identifier: CA372228576
Gene: TG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132948928C>A , CM000670.2:g.132948928C>A GRCh38
NC_000008.10:g.133961173C>A , CM000670.1:g.133961173C>A GRCh37
NC_000008.9:g.134030355C>A NCBI36
NG_015832.1:g.86969C>A

Transcript Alleles

HGVS Amino-acid Change
NM_003235.5:c.5386C>A MANE Select NP_003226.4:p.Gln1796Lys
ENST00000220616.9:c.5386C>A MANE Select ENSP00000220616.4:p.Gln1796Lys
NM_003235.4:c.5386C>A NP_003226.4:p.Gln1796Lys
ENST00000220616.8:c.5386C>A ENSP00000220616.4:p.Gln1796Lys
ENST00000519178.5:c.752C>A
ENST00000523756.5:c.2041C>A
XM_005251038.3:c.5194C>A XP_005251095.1:p.Gln1732Lys
XM_005251038.4:c.5194C>A XP_005251095.1:p.Gln1732Lys
XM_005251040.3:c.5386C>A XP_005251097.1:p.Gln1796Lys
XM_005251040.4:c.5386C>A XP_005251097.1:p.Gln1796Lys
XM_005251042.3:c.5386C>A XP_005251099.1:p.Gln1796Lys
XM_005251042.4:c.5386C>A XP_005251099.1:p.Gln1796Lys
XM_005251043.3:c.5386C>A XP_005251100.1:p.Gln1796Lys
XM_006716622.2:c.5386C>A XP_006716685.1:p.Gln1796Lys
XM_006716622.3:c.5386C>A XP_006716685.1:p.Gln1796Lys
XM_017013793.1:c.5386C>A XP_016869282.1:p.Gln1796Lys
XM_017013794.1:c.5386C>A XP_016869283.1:p.Gln1796Lys
XM_017013795.1:c.5215C>A XP_016869284.1:p.Gln1739Lys
XM_017013796.1:c.5167C>A XP_016869285.1:p.Gln1723Lys
XM_017013797.1:c.5125C>A XP_016869286.1:p.Gln1709Lys
XM_017013798.1:c.5386C>A XP_016869287.1:p.Gln1796Lys
XM_017013799.1:c.5386C>A XP_016869288.1:p.Gln1796Lys
XM_017013800.1:c.5386C>A XP_016869289.1:p.Gln1796Lys