Canonical Allele Identifier: CA2613377303

Gene: DDB2

Linked Data

• gnomAD v4: 11-47234936-T-TTTCA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234936_47234937insTTCA , CM000673.2:g.47234936_47234937insTTCA	GRCh38
NC_000011.9:g.47256487_47256488insTTCA , CM000673.1:g.47256487_47256488insTTCA	GRCh37
NC_000011.8:g.47213063_47213064insTTCA	NCBI36
NG_009365.1:g.24995_24996insTTCA , LRG_467:g.24995_24996insTTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.880+2_880+3insTTCA MANE Select	ENSP00000256996.4:n.880+2_880+3insTTCA
ENST00000256996.8:c.880+2_880+3insTTCA	ENSP00000256996.3:n.880+2_880+3insTTCA
ENST00000378600.7:c.457-2901_457-2900insTTCA	ENSP00000367863.3:n.457-2901_457-2900insTTCA
ENST00000378601.7:c.702+264_702+265insTTCA	ENSP00000367864.3:n.702+264_702+265insTTCA
ENST00000378603.7:c.688+2_688+3insTTCA	ENSP00000367866.3:n.688+2_688+3insTTCA
ENST00000612309.4:n.1996_1997insTTCA
ENST00000614394.1:n.270+2_270+3insTTCA
ENST00000616278.4:c.556+264_556+265insTTCA	ENSP00000478411.1:n.556+264_556+265insTTCA
ENST00000617022.4:n.1554-2901_1554-2900insTTCA
ENST00000617847.4:c.809+2_809+3insTTCA
ENST00000620515.1:n.46+264_46+265insTTCA
NM_000107.2:c.880+2_880+3insTTCA , LRG_467t1:c.880+2_880+3insTTCA	NP_000098.1:n.880+2_880+3insTTCA
NM_001300734.1:c.457-2901_457-2900insTTCA	NP_001287663.1:n.457-2901_457-2900insTTCA
XR_242780.3:n.870+264_870+265insTTCA
XR_242780.4:n.870+264_870+265insTTCA
NM_000107.3:c.880+2_880+3insTTCA MANE Select	NP_000098.1:n.880+2_880+3insTTCA
NM_001300734.2:c.457-2901_457-2900insTTCA	NP_001287663.1:n.457-2901_457-2900insTTCA
NM_001399874.1:c.880+2_880+3insTTCA	NP_001386803.1:n.880+2_880+3insTTCA
NM_001399875.1:c.880+2_880+3insTTCA	NP_001386804.1:n.880+2_880+3insTTCA
NM_001399876.1:c.457-2901_457-2900insTTCA	NP_001386805.1:n.457-2901_457-2900insTTCA
NM_001399878.1:c.688+2_688+3insTTCA	NP_001386807.1:n.688+2_688+3insTTCA
NR_174610.1:n.1131+264_1131+265insTTCA
NR_174611.1:n.1109+60_1109+61insTTCA