Canonical Allele Identifier: CA2059947032

Gene: TDG

Linked Data

• dbSNP Id: rs1871598513

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.103977497G>T , CM000674.2:g.103977497G>T	GRCh38
NC_000012.11:g.104371275G>T , CM000674.1:g.104371275G>T	GRCh37
NC_000012.10:g.102895405G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392872.8:c.166+437G>T MANE Select	ENSP00000376611.3:n.166+437G>T
ENST00000266775.13:c.154+437G>T	ENSP00000266775.9:n.154+437G>T
ENST00000392872.7:c.166+437G>T	ENSP00000376611.3:n.166+437G>T
ENST00000436021.6:c.91+437G>T	ENSP00000390167.2:n.91+437G>T
ENST00000537100.5:c.166+437G>T	ENSP00000439825.1:n.166+437G>T
ENST00000544060.1:n.301+437G>T
ENST00000544861.5:c.-263-2334G>T	ENSP00000445899.1:n.-263-2334G>T
ENST00000545698.1:n.220-2334G>T
NM_003211.4:c.166+437G>T	NP_003202.3:n.166+437G>T
XM_005269125.1:c.-364+437G>T	XP_005269182.1:n.-364+437G>T
XM_011538714.1:c.-263-2334G>T	XP_011537016.1:n.-263-2334G>T
XM_011538715.1:c.-363-2334G>T	XP_011537017.1:n.-363-2334G>T
XR_429113.1:n.389+437G>T
NM_001363612.1:c.-263-2334G>T	NP_001350541.1:n.-263-2334G>T
NM_003211.5:c.166+437G>T	NP_003202.3:n.166+437G>T
XM_005269125.2:c.-364+437G>T	XP_005269182.1:n.-364+437G>T
NM_003211.6:c.166+437G>T MANE Select	NP_003202.3:n.166+437G>T
NM_001363612.2:c.-263-2334G>T	NP_001350541.1:n.-263-2334G>T