Canonical Allele Identifier: CA2059947052

Gene: TDG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.103977536_103977538delinsCAG , CM000674.2:g.103977536_103977538delinsCAG	GRCh38
NC_000012.11:g.104371314_104371316delinsCAG , CM000674.1:g.104371314_104371316delinsCAG	GRCh37
NC_000012.10:g.102895444_102895446delinsCAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392872.8:c.166+476_166+478delinsCAG MANE Select	ENSP00000376611.3:n.166+476_166+478delinsCAG
ENST00000266775.13:c.154+476_154+478delinsCAG	ENSP00000266775.9:n.154+476_154+478delinsCAG
ENST00000392872.7:c.166+476_166+478delinsCAG	ENSP00000376611.3:n.166+476_166+478delinsCAG
ENST00000436021.6:c.91+476_91+478delinsCAG	ENSP00000390167.2:n.91+476_91+478delinsCAG
ENST00000537100.5:c.166+476_166+478delinsCAG	ENSP00000439825.1:n.166+476_166+478delinsCAG
ENST00000544060.1:n.301+476_301+478delinsCAG
ENST00000544861.5:c.-263-2295_-263-2293delinsCAG	ENSP00000445899.1:n.-263-2295_-263-2293delinsCAG
ENST00000545698.1:n.220-2295_220-2293delinsCAG
NM_003211.4:c.166+476_166+478delinsCAG	NP_003202.3:n.166+476_166+478delinsCAG
XM_005269125.1:c.-364+476_-364+478delinsCAG	XP_005269182.1:n.-364+476_-364+478delinsCAG
XM_011538714.1:c.-263-2295_-263-2293delinsCAG	XP_011537016.1:n.-263-2295_-263-2293delinsCAG
XM_011538715.1:c.-363-2295_-363-2293delinsCAG	XP_011537017.1:n.-363-2295_-363-2293delinsCAG
XR_429113.1:n.389+476_389+478delinsCAG
NM_001363612.1:c.-263-2295_-263-2293delinsCAG	NP_001350541.1:n.-263-2295_-263-2293delinsCAG
NM_003211.5:c.166+476_166+478delinsCAG	NP_003202.3:n.166+476_166+478delinsCAG
XM_005269125.2:c.-364+476_-364+478delinsCAG	XP_005269182.1:n.-364+476_-364+478delinsCAG
NM_003211.6:c.166+476_166+478delinsCAG MANE Select	NP_003202.3:n.166+476_166+478delinsCAG
NM_001363612.2:c.-263-2295_-263-2293delinsCAG	NP_001350541.1:n.-263-2295_-263-2293delinsCAG