Canonical Allele Identifier: CA607172658

Gene: TDG

Linked Data

• dbSNP Id: rs1423735258
• gnomAD v2: 12-104371419-T-C
• gnomAD v3: 12-103977641-T-C
• gnomAD v4: 12-103977641-T-C
• MyVariant Identifiers: chr12:g.104371419T>C (hg19) ; chr12:g.103977641T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.103977641T>C , CM000674.2:g.103977641T>C	GRCh38
NC_000012.11:g.104371419T>C , CM000674.1:g.104371419T>C	GRCh37
NC_000012.10:g.102895549T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392872.8:c.166+581T>C MANE Select	ENSP00000376611.3:n.166+581T>C
ENST00000266775.13:c.154+581T>C	ENSP00000266775.9:n.154+581T>C
ENST00000392872.7:c.166+581T>C	ENSP00000376611.3:n.166+581T>C
ENST00000436021.6:c.91+581T>C	ENSP00000390167.2:n.91+581T>C
ENST00000537100.5:c.166+581T>C	ENSP00000439825.1:n.166+581T>C
ENST00000544060.1:n.301+581T>C
ENST00000544861.5:c.-263-2190T>C	ENSP00000445899.1:n.-263-2190T>C
ENST00000545698.1:n.220-2190T>C
NM_003211.4:c.166+581T>C	NP_003202.3:n.166+581T>C
XM_005269125.1:c.-364+581T>C	XP_005269182.1:n.-364+581T>C
XM_011538714.1:c.-263-2190T>C	XP_011537016.1:n.-263-2190T>C
XM_011538715.1:c.-363-2190T>C	XP_011537017.1:n.-363-2190T>C
XR_429113.1:n.389+581T>C
NM_001363612.1:c.-263-2190T>C	NP_001350541.1:n.-263-2190T>C
NM_003211.5:c.166+581T>C	NP_003202.3:n.166+581T>C
XM_005269125.2:c.-364+581T>C	XP_005269182.1:n.-364+581T>C
NM_003211.6:c.166+581T>C MANE Select	NP_003202.3:n.166+581T>C
NM_001363612.2:c.-263-2190T>C	NP_001350541.1:n.-263-2190T>C