Canonical Allele Identifier: CA221687306
Gene: DDB2 HGNC NCBI

Linked Data

dbSNP Id: rs143615033

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47235078_47235079insGGGG , CM000673.2:g.47235078_47235079insGGGG GRCh38
NC_000011.9:g.47256629_47256630insGGGG , CM000673.1:g.47256629_47256630insGGGG GRCh37
NC_000011.8:g.47213205_47213206insGGGG NCBI36
NG_009365.1:g.25137_25138insGGGG , LRG_467:g.25137_25138insGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000256996.9:c.880+144_880+145insGGGG MANE Select ENSP00000256996.4:n.880+144_880+145insGGGG
ENST00000256996.8:c.880+144_880+145insGGGG ENSP00000256996.3:n.880+144_880+145insGGGG
ENST00000378600.7:c.457-2759_457-2758insGGGG ENSP00000367863.3:n.457-2759_457-2758insGGGG
ENST00000378601.7:c.703-192_703-191insGGGG ENSP00000367864.3:n.703-192_703-191insGGGG
ENST00000378603.7:c.688+144_688+145insGGGG ENSP00000367866.3:n.688+144_688+145insGGGG
ENST00000612309.4:n.2138_2139insGGGG
ENST00000614394.1:n.270+144_270+145insGGGG
ENST00000616278.4:c.557-192_557-191insGGGG ENSP00000478411.1:n.557-192_557-191insGGGG
ENST00000617022.4:n.1554-2759_1554-2758insGGGG
ENST00000617847.4:c.809+144_809+145insGGGG
ENST00000620515.1:n.47-192_47-191insGGGG
NM_000107.2:c.880+144_880+145insGGGG , LRG_467t1:c.880+144_880+145insGGGG NP_000098.1:n.880+144_880+145insGGGG
NM_001300734.1:c.457-2759_457-2758insGGGG NP_001287663.1:n.457-2759_457-2758insGGGG
XR_242780.3:n.871-192_871-191insGGGG
XR_242780.4:n.871-192_871-191insGGGG
NM_000107.3:c.880+144_880+145insGGGG MANE Select NP_000098.1:n.880+144_880+145insGGGG
NM_001300734.2:c.457-2759_457-2758insGGGG NP_001287663.1:n.457-2759_457-2758insGGGG
NM_001399874.1:c.880+144_880+145insGGGG NP_001386803.1:n.880+144_880+145insGGGG
NM_001399875.1:c.880+144_880+145insGGGG NP_001386804.1:n.880+144_880+145insGGGG
NM_001399876.1:c.457-2759_457-2758insGGGG NP_001386805.1:n.457-2759_457-2758insGGGG
NM_001399878.1:c.688+144_688+145insGGGG NP_001386807.1:n.688+144_688+145insGGGG
NR_174610.1:n.1132-192_1132-191insGGGG
NR_174611.1:n.1110-192_1110-191insGGGG