Canonical Allele Identifier: CA2579255374
Gene: TG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133133484del , CM000670.2:g.133133484del GRCh38
NC_000008.10:g.134145728del , CM000670.1:g.134145728del GRCh37
NC_000008.9:g.134214910del NCBI36
NG_015832.1:g.271524del

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.8012del MANE Select ENSP00000220616.4:p.Pro2671LeufsTer?
ENST00000220616.8:c.8012del ENSP00000220616.4:p.Pro2671LeufsTer?
ENST00000519178.5:c.3378del
ENST00000519543.5:c.2411del ENSP00000430430.1:p.Pro804LeufsTer?
ENST00000521107.1:c.224del ENSP00000430161.1:p.Pro75LeufsTer?
ENST00000522691.1:n.98del
ENST00000523756.5:c.4667del
NM_003235.4:c.8012del NP_003226.4:p.Pro2671LeufsTer?
XM_005251038.3:c.7820del XP_005251095.1:p.Pro2607LeufsTer?
XM_006716622.2:c.7949del XP_006716685.1:p.Pro2650LeufsTer?
XM_005251038.4:c.7820del XP_005251095.1:p.Pro2607LeufsTer?
XM_006716622.3:c.7949del XP_006716685.1:p.Pro2650LeufsTer?
XM_017013793.1:c.7946del XP_016869282.1:p.Pro2649LeufsTer?
XM_017013794.1:c.7877del XP_016869283.1:p.Pro2626LeufsTer?
XM_017013795.1:c.7841del XP_016869284.1:p.Pro2614LeufsTer?
XM_017013796.1:c.7793del XP_016869285.1:p.Pro2598LeufsTer?
XM_017013797.1:c.7751del XP_016869286.1:p.Pro2584LeufsTer?
NM_003235.5:c.8012del MANE Select NP_003226.4:p.Pro2671LeufsTer?