Canonical Allele Identifier: CA372253681
Gene: TG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133133648A>T , CM000670.2:g.133133648A>T GRCh38
NC_000008.10:g.134145892A>T , CM000670.1:g.134145892A>T GRCh37
NC_000008.9:g.134215074A>T NCBI36
NG_015832.1:g.271688A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.8176A>T MANE Select ENSP00000220616.4:p.Lys2726Ter
ENST00000220616.8:c.8176A>T ENSP00000220616.4:p.Lys2726Ter
ENST00000519178.5:c.3542A>T
ENST00000519543.5:c.2575A>T ENSP00000430430.1:p.Lys859Ter
ENST00000521107.1:c.388A>T ENSP00000430161.1:p.Lys130Ter
ENST00000522691.1:n.262A>T
ENST00000523756.5:c.4831A>T
NM_003235.4:c.8176A>T NP_003226.4:p.Lys2726Ter
XM_005251038.3:c.7984A>T XP_005251095.1:p.Lys2662Ter
XM_006716622.2:c.8113A>T XP_006716685.1:p.Lys2705Ter
XM_005251038.4:c.7984A>T XP_005251095.1:p.Lys2662Ter
XM_006716622.3:c.8113A>T XP_006716685.1:p.Lys2705Ter
XM_017013793.1:c.8110A>T XP_016869282.1:p.Lys2704Ter
XM_017013794.1:c.8041A>T XP_016869283.1:p.Lys2681Ter
XM_017013795.1:c.8005A>T XP_016869284.1:p.Lys2669Ter
XM_017013796.1:c.7957A>T XP_016869285.1:p.Lys2653Ter
XM_017013797.1:c.7915A>T XP_016869286.1:p.Lys2639Ter
NM_003235.5:c.8176A>T MANE Select NP_003226.4:p.Lys2726Ter