Canonical Allele Identifier: CA2613377575

Gene: DDB2

Linked Data

• gnomAD v4: 11-47235035-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235036_47235037dup , CM000673.2:g.47235036_47235037dup	GRCh38
NC_000011.9:g.47256587_47256588dup , CM000673.1:g.47256587_47256588dup	GRCh37
NC_000011.8:g.47213163_47213164dup	NCBI36
NG_009365.1:g.25095_25096dup , LRG_467:g.25095_25096dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.880+102_880+103dup MANE Select	ENSP00000256996.4:n.880+102_880+103dup
ENST00000256996.8:c.880+102_880+103dup	ENSP00000256996.3:n.880+102_880+103dup
ENST00000378600.7:c.457-2801_457-2800dup	ENSP00000367863.3:n.457-2801_457-2800dup
ENST00000378601.7:c.703-234_703-233dup	ENSP00000367864.3:n.703-234_703-233dup
ENST00000378603.7:c.688+102_688+103dup	ENSP00000367866.3:n.688+102_688+103dup
ENST00000612309.4:n.2096_2097dup
ENST00000614394.1:n.270+102_270+103dup
ENST00000616278.4:c.557-234_557-233dup	ENSP00000478411.1:n.557-234_557-233dup
ENST00000617022.4:n.1554-2801_1554-2800dup
ENST00000617847.4:c.809+102_809+103dup
ENST00000620515.1:n.47-234_47-233dup
NM_000107.2:c.880+102_880+103dup , LRG_467t1:c.880+102_880+103dup	NP_000098.1:n.880+102_880+103dup
NM_001300734.1:c.457-2801_457-2800dup	NP_001287663.1:n.457-2801_457-2800dup
XR_242780.3:n.871-234_871-233dup
XR_242780.4:n.871-234_871-233dup
NM_000107.3:c.880+102_880+103dup MANE Select	NP_000098.1:n.880+102_880+103dup
NM_001300734.2:c.457-2801_457-2800dup	NP_001287663.1:n.457-2801_457-2800dup
NM_001399874.1:c.880+102_880+103dup	NP_001386803.1:n.880+102_880+103dup
NM_001399875.1:c.880+102_880+103dup	NP_001386804.1:n.880+102_880+103dup
NM_001399876.1:c.457-2801_457-2800dup	NP_001386805.1:n.457-2801_457-2800dup
NM_001399878.1:c.688+102_688+103dup	NP_001386807.1:n.688+102_688+103dup
NR_174610.1:n.1132-234_1132-233dup
NR_174611.1:n.1109+160_1109+161dup