Canonical Allele Identifier: CA2613377298

Gene: DDB2

Linked Data

• gnomAD v4: 11-47234934-G-GCTT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47234934_47234935insCTT , CM000673.2:g.47234934_47234935insCTT	GRCh38
NC_000011.9:g.47256485_47256486insCTT , CM000673.1:g.47256485_47256486insCTT	GRCh37
NC_000011.8:g.47213061_47213062insCTT	NCBI36
NG_009365.1:g.24993_24994insCTT , LRG_467:g.24993_24994insCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.880_880+1insCTT MANE Select	ENSP00000256996.4:n.880_880+1insCTT
ENST00000256996.8:c.880_880+1insCTT	ENSP00000256996.3:n.880_880+1insCTT
ENST00000378600.7:c.457-2903_457-2902insCTT	ENSP00000367863.3:n.457-2903_457-2902insCTT
ENST00000378601.7:c.702+262_702+263insCTT	ENSP00000367864.3:n.702+262_702+263insCTT
ENST00000378603.7:c.688_688+1insCTT	ENSP00000367866.3:n.688_688+1insCTT
ENST00000612309.4:n.1994_1995insCTT
ENST00000614394.1:n.270_270+1insCTT
ENST00000616278.4:c.556+262_556+263insCTT	ENSP00000478411.1:n.556+262_556+263insCTT
ENST00000617022.4:n.1554-2903_1554-2902insCTT
ENST00000617847.4:c.809_809+1insCTT
ENST00000620515.1:n.46+262_46+263insCTT
NM_000107.2:c.880_880+1insCTT , LRG_467t1:c.880_880+1insCTT	NP_000098.1:n.880_880+1insCTT
NM_001300734.1:c.457-2903_457-2902insCTT	NP_001287663.1:n.457-2903_457-2902insCTT
XR_242780.3:n.870+262_870+263insCTT
XR_242780.4:n.870+262_870+263insCTT
NM_000107.3:c.880_880+1insCTT MANE Select	NP_000098.1:n.880_880+1insCTT
NM_001300734.2:c.457-2903_457-2902insCTT	NP_001287663.1:n.457-2903_457-2902insCTT
NM_001399874.1:c.880_880+1insCTT	NP_001386803.1:n.880_880+1insCTT
NM_001399875.1:c.880_880+1insCTT	NP_001386804.1:n.880_880+1insCTT
NM_001399876.1:c.457-2903_457-2902insCTT	NP_001386805.1:n.457-2903_457-2902insCTT
NM_001399878.1:c.688_688+1insCTT	NP_001386807.1:n.688_688+1insCTT
NR_174610.1:n.1131+262_1131+263insCTT
NR_174611.1:n.1109+58_1109+59insCTT