Canonical Allele Identifier: CA951314571
Gene: TDG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.103977491_103977493del , CM000674.2:g.103977491_103977493del GRCh38
NC_000012.11:g.104371269_104371271del , CM000674.1:g.104371269_104371271del GRCh37
NC_000012.10:g.102895399_102895401del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000392872.8:c.166+431_166+433del MANE Select ENSP00000376611.3:n.166+431_166+433del
ENST00000266775.13:c.154+431_154+433del ENSP00000266775.9:n.154+431_154+433del
ENST00000392872.7:c.166+431_166+433del ENSP00000376611.3:n.166+431_166+433del
ENST00000436021.6:c.91+431_91+433del ENSP00000390167.2:n.91+431_91+433del
ENST00000537100.5:c.166+431_166+433del ENSP00000439825.1:n.166+431_166+433del
ENST00000544060.1:n.301+431_301+433del
ENST00000544861.5:c.-263-2340_-263-2338del ENSP00000445899.1:n.-263-2340_-263-2338del
ENST00000545698.1:n.220-2340_220-2338del
NM_003211.4:c.166+431_166+433del NP_003202.3:n.166+431_166+433del
XM_005269125.1:c.-364+431_-364+433del XP_005269182.1:n.-364+431_-364+433del
XM_011538714.1:c.-263-2340_-263-2338del XP_011537016.1:n.-263-2340_-263-2338del
XM_011538715.1:c.-363-2340_-363-2338del XP_011537017.1:n.-363-2340_-363-2338del
XR_429113.1:n.389+431_389+433del
NM_001363612.1:c.-263-2340_-263-2338del NP_001350541.1:n.-263-2340_-263-2338del
NM_003211.5:c.166+431_166+433del NP_003202.3:n.166+431_166+433del
XM_005269125.2:c.-364+431_-364+433del XP_005269182.1:n.-364+431_-364+433del
NM_003211.6:c.166+431_166+433del MANE Select NP_003202.3:n.166+431_166+433del
NM_001363612.2:c.-263-2340_-263-2338del NP_001350541.1:n.-263-2340_-263-2338del