Canonical Allele Identifier: CA1969296787

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235034_47235036delinsCCT , CM000673.2:g.47235034_47235036delinsCCT	GRCh38
NC_000011.9:g.47256585_47256587delinsCCT , CM000673.1:g.47256585_47256587delinsCCT	GRCh37
NC_000011.8:g.47213161_47213163delinsCCT	NCBI36
NG_009365.1:g.25093_25095delinsCCT , LRG_467:g.25093_25095delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.880+100_880+102delinsCCT MANE Select	ENSP00000256996.4:n.880+100_880+102delinsCCT
ENST00000256996.8:c.880+100_880+102delinsCCT	ENSP00000256996.3:n.880+100_880+102delinsCCT
ENST00000378600.7:c.457-2803_457-2801delinsCCT	ENSP00000367863.3:n.457-2803_457-2801delinsCCT
ENST00000378601.7:c.703-236_703-234delinsCCT	ENSP00000367864.3:n.703-236_703-234delinsCCT
ENST00000378603.7:c.688+100_688+102delinsCCT	ENSP00000367866.3:n.688+100_688+102delinsCCT
ENST00000612309.4:n.2094_2096delinsCCT
ENST00000614394.1:n.270+100_270+102delinsCCT
ENST00000616278.4:c.557-236_557-234delinsCCT	ENSP00000478411.1:n.557-236_557-234delinsCCT
ENST00000617022.4:n.1554-2803_1554-2801delinsCCT
ENST00000617847.4:c.809+100_809+102delinsCCT
ENST00000620515.1:n.47-236_47-234delinsCCT
NM_000107.2:c.880+100_880+102delinsCCT , LRG_467t1:c.880+100_880+102delinsCCT	NP_000098.1:n.880+100_880+102delinsCCT
NM_001300734.1:c.457-2803_457-2801delinsCCT	NP_001287663.1:n.457-2803_457-2801delinsCCT
XR_242780.3:n.871-236_871-234delinsCCT
XR_242780.4:n.871-236_871-234delinsCCT
NM_000107.3:c.880+100_880+102delinsCCT MANE Select	NP_000098.1:n.880+100_880+102delinsCCT
NM_001300734.2:c.457-2803_457-2801delinsCCT	NP_001287663.1:n.457-2803_457-2801delinsCCT
NM_001399874.1:c.880+100_880+102delinsCCT	NP_001386803.1:n.880+100_880+102delinsCCT
NM_001399875.1:c.880+100_880+102delinsCCT	NP_001386804.1:n.880+100_880+102delinsCCT
NM_001399876.1:c.457-2803_457-2801delinsCCT	NP_001386805.1:n.457-2803_457-2801delinsCCT
NM_001399878.1:c.688+100_688+102delinsCCT	NP_001386807.1:n.688+100_688+102delinsCCT
NR_174610.1:n.1132-236_1132-234delinsCCT
NR_174611.1:n.1109+158_1109+160delinsCCT