Canonical Allele Identifier: CA242540695

Gene: TDG

Linked Data

• dbSNP Id: rs773684574
• gnomAD v3: 12-103977536-CAG-C
• gnomAD v4: 12-103977536-CAG-C
• MyVariant Identifiers: chr12:g.104371315_104371316del (hg19) ; chr12:g.103977537_103977538del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.103977539_103977540del , CM000674.2:g.103977539_103977540del	GRCh38
NC_000012.11:g.104371317_104371318del , CM000674.1:g.104371317_104371318del	GRCh37
NC_000012.10:g.102895447_102895448del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000392872.8:c.166+479_166+480del MANE Select	ENSP00000376611.3:n.166+479_166+480del
ENST00000266775.13:c.154+479_154+480del	ENSP00000266775.9:n.154+479_154+480del
ENST00000392872.7:c.166+479_166+480del	ENSP00000376611.3:n.166+479_166+480del
ENST00000436021.6:c.91+479_91+480del	ENSP00000390167.2:n.91+479_91+480del
ENST00000537100.5:c.166+479_166+480del	ENSP00000439825.1:n.166+479_166+480del
ENST00000544060.1:n.301+479_301+480del
ENST00000544861.5:c.-263-2292_-263-2291del	ENSP00000445899.1:n.-263-2292_-263-2291del
ENST00000545698.1:n.220-2292_220-2291del
NM_003211.4:c.166+479_166+480del	NP_003202.3:n.166+479_166+480del
XM_005269125.1:c.-364+479_-364+480del	XP_005269182.1:n.-364+479_-364+480del
XM_011538714.1:c.-263-2292_-263-2291del	XP_011537016.1:n.-263-2292_-263-2291del
XM_011538715.1:c.-363-2292_-363-2291del	XP_011537017.1:n.-363-2292_-363-2291del
XR_429113.1:n.389+479_389+480del
NM_001363612.1:c.-263-2292_-263-2291del	NP_001350541.1:n.-263-2292_-263-2291del
NM_003211.5:c.166+479_166+480del	NP_003202.3:n.166+479_166+480del
XM_005269125.2:c.-364+479_-364+480del	XP_005269182.1:n.-364+479_-364+480del
NM_003211.6:c.166+479_166+480del MANE Select	NP_003202.3:n.166+479_166+480del
NM_001363612.2:c.-263-2292_-263-2291del	NP_001350541.1:n.-263-2292_-263-2291del