Canonical Allele Identifier: CA1821005068
Gene: TG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132971846G= , CM000670.2:g.132971846G= GRCh38
NC_000008.10:g.133984091G= , CM000670.1:g.133984091G= GRCh37
NC_000008.9:g.134053273G= NCBI36
NG_015832.1:g.109887G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.6028G= MANE Select ENSP00000220616.4:p.Gly2010=
ENST00000220616.8:c.6028G= ENSP00000220616.4:p.Gly2010=
ENST00000519178.5:c.1394G=
ENST00000519294.5:n.20G=
ENST00000519543.5:c.490G= ENSP00000430430.1:p.Gly164=
ENST00000520089.5:n.137G=
ENST00000520197.5:n.165G=
ENST00000523756.5:c.2683G=
NM_003235.4:c.6028G= NP_003226.4:p.Gly2010=
XM_005251038.3:c.5836G= XP_005251095.1:p.Gly1946=
XM_005251040.3:c.6028G= XP_005251097.1:p.Gly2010=
XM_005251042.3:c.6028G= XP_005251099.1:p.Gly2010=
XM_005251043.3:c.6028G= XP_005251100.1:p.Gly2010=
XM_006716622.2:c.6028G= XP_006716685.1:p.Gly2010=
XM_005251038.4:c.5836G= XP_005251095.1:p.Gly1946=
XM_005251040.4:c.6028G= XP_005251097.1:p.Gly2010=
XM_005251042.4:c.6028G= XP_005251099.1:p.Gly2010=
XM_006716622.3:c.6028G= XP_006716685.1:p.Gly2010=
XM_017013793.1:c.5962G= XP_016869282.1:p.Gly1988=
XM_017013794.1:c.6028G= XP_016869283.1:p.Gly2010=
XM_017013795.1:c.5857G= XP_016869284.1:p.Gly1953=
XM_017013796.1:c.5809G= XP_016869285.1:p.Gly1937=
XM_017013797.1:c.5767G= XP_016869286.1:p.Gly1923=
XM_017013798.1:c.6028G= XP_016869287.1:p.Gly2010=
XM_017013799.1:c.6028G= XP_016869288.1:p.Gly2010=
XM_017013800.1:c.6028G= XP_016869289.1:p.Gly2010=
NM_003235.5:c.6028G= MANE Select NP_003226.4:p.Gly2010=