Canonical Allele Identifier: CA682957925

Gene: TDG

Linked Data

• dbSNP Id: rs1484798163
• gnomAD v3: 12-103977587-AGG-A
• gnomAD v4: 12-103977587-AGG-A
• MyVariant Identifiers: chr12:g.104371366_104371367del (hg19) ; chr12:g.103977588_103977589del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.103977588_103977589del , CM000674.2:g.103977588_103977589del	GRCh38
NC_000012.11:g.104371366_104371367del , CM000674.1:g.104371366_104371367del	GRCh37
NC_000012.10:g.102895496_102895497del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392872.8:c.166+528_166+529del MANE Select	ENSP00000376611.3:n.166+528_166+529del
ENST00000266775.13:c.154+528_154+529del	ENSP00000266775.9:n.154+528_154+529del
ENST00000392872.7:c.166+528_166+529del	ENSP00000376611.3:n.166+528_166+529del
ENST00000436021.6:c.91+528_91+529del	ENSP00000390167.2:n.91+528_91+529del
ENST00000537100.5:c.166+528_166+529del	ENSP00000439825.1:n.166+528_166+529del
ENST00000544060.1:n.301+528_301+529del
ENST00000544861.5:c.-263-2243_-263-2242del	ENSP00000445899.1:n.-263-2243_-263-2242del
ENST00000545698.1:n.220-2243_220-2242del
NM_003211.4:c.166+528_166+529del	NP_003202.3:n.166+528_166+529del
XM_005269125.1:c.-364+528_-364+529del	XP_005269182.1:n.-364+528_-364+529del
XM_011538714.1:c.-263-2243_-263-2242del	XP_011537016.1:n.-263-2243_-263-2242del
XM_011538715.1:c.-363-2243_-363-2242del	XP_011537017.1:n.-363-2243_-363-2242del
XR_429113.1:n.389+528_389+529del
NM_001363612.1:c.-263-2243_-263-2242del	NP_001350541.1:n.-263-2243_-263-2242del
NM_003211.5:c.166+528_166+529del	NP_003202.3:n.166+528_166+529del
XM_005269125.2:c.-364+528_-364+529del	XP_005269182.1:n.-364+528_-364+529del
NM_003211.6:c.166+528_166+529del MANE Select	NP_003202.3:n.166+528_166+529del
NM_001363612.2:c.-263-2243_-263-2242del	NP_001350541.1:n.-263-2243_-263-2242del