Canonical Allele Identifier: CA1821104980
Gene: TG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133133660_133133662delinsGGT , CM000670.2:g.133133660_133133662delinsGGT GRCh38
NC_000008.10:g.134145904_134145906delinsGGT , CM000670.1:g.134145904_134145906delinsGGT GRCh37
NC_000008.9:g.134215086_134215088delinsGGT NCBI36
NG_015832.1:g.271700_271702delinsGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.8188_8188+2delinsGGT
ENST00000220616.8:c.8188_8188+2delinsGGT
ENST00000519178.5:c.3554_3554+2delinsGGT
ENST00000519543.5:c.2587_2587+2delinsGGT
ENST00000521107.1:c.400_400+2delinsGGT
ENST00000522691.1:n.274_274+2delinsGGT
ENST00000523756.5:c.4843_4843+2delinsGGT
NM_003235.4:c.8188_8188+2delinsGGT
XM_005251038.3:c.7996_7996+2delinsGGT
XM_006716622.2:c.8125_8125+2delinsGGT
XM_005251038.4:c.7996_7996+2delinsGGT
XM_006716622.3:c.8125_8125+2delinsGGT
XM_017013793.1:c.8122_8122+2delinsGGT
XM_017013794.1:c.8053_8053+2delinsGGT
XM_017013795.1:c.8017_8017+2delinsGGT
XM_017013796.1:c.7969_7969+2delinsGGT
XM_017013797.1:c.7927_7927+2delinsGGT
NM_003235.5:c.8188_8188+2delinsGGT