Canonical Allele Identifier: CA2791322868

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235003_47235004del , CM000673.2:g.47235003_47235004del	GRCh38
NC_000011.9:g.47256554_47256555del , CM000673.1:g.47256554_47256555del	GRCh37
NC_000011.8:g.47213130_47213131del	NCBI36
NG_009365.1:g.25062_25063del , LRG_467:g.25062_25063del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.880+69_880+70del MANE Select	ENSP00000256996.4:n.880+69_880+70del
ENST00000256996.8:c.880+69_880+70del	ENSP00000256996.3:n.880+69_880+70del
ENST00000378600.7:c.457-2834_457-2833del	ENSP00000367863.3:n.457-2834_457-2833del
ENST00000378601.7:c.703-267_703-266del	ENSP00000367864.3:n.703-267_703-266del
ENST00000378603.7:c.688+69_688+70del	ENSP00000367866.3:n.688+69_688+70del
ENST00000612309.4:n.2063_2064del
ENST00000614394.1:n.270+69_270+70del
ENST00000616278.4:c.557-267_557-266del	ENSP00000478411.1:n.557-267_557-266del
ENST00000617022.4:n.1554-2834_1554-2833del
ENST00000617847.4:c.809+69_809+70del
ENST00000620515.1:n.47-267_47-266del
NM_000107.2:c.880+69_880+70del , LRG_467t1:c.880+69_880+70del	NP_000098.1:n.880+69_880+70del
NM_001300734.1:c.457-2834_457-2833del	NP_001287663.1:n.457-2834_457-2833del
XR_242780.3:n.871-267_871-266del
XR_242780.4:n.871-267_871-266del
NM_000107.3:c.880+69_880+70del MANE Select	NP_000098.1:n.880+69_880+70del
NM_001300734.2:c.457-2834_457-2833del	NP_001287663.1:n.457-2834_457-2833del
NM_001399874.1:c.880+69_880+70del	NP_001386803.1:n.880+69_880+70del
NM_001399875.1:c.880+69_880+70del	NP_001386804.1:n.880+69_880+70del
NM_001399876.1:c.457-2834_457-2833del	NP_001386805.1:n.457-2834_457-2833del
NM_001399878.1:c.688+69_688+70del	NP_001386807.1:n.688+69_688+70del
NR_174610.1:n.1132-267_1132-266del
NR_174611.1:n.1109+127_1109+128del