Canonical Allele Identifier: CA2613379425
Gene: DDB2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47235568_47235569dup , CM000673.2:g.47235568_47235569dup GRCh38
NC_000011.9:g.47257119_47257120dup , CM000673.1:g.47257119_47257120dup GRCh37
NC_000011.8:g.47213695_47213696dup NCBI36
NG_009365.1:g.25627_25628dup , LRG_467:g.25627_25628dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000256996.9:c.1023+156_1023+157dup MANE Select ENSP00000256996.4:n.1023+156_1023+157dup
ENST00000256996.8:c.1023+156_1023+157dup ENSP00000256996.3:n.1023+156_1023+157dup
ENST00000378600.7:c.457-2269_457-2268dup ENSP00000367863.3:n.457-2269_457-2268dup
ENST00000378601.7:c.*110+156_*110+157dup ENSP00000367864.3:n.*110+156_*110+157dup
ENST00000378603.7:c.831+156_831+157dup ENSP00000367866.3:n.831+156_831+157dup
ENST00000612309.4:n.2472+156_2472+157dup
ENST00000614394.1:n.569_570dup
ENST00000616278.4:c.699+156_699+157dup ENSP00000478411.1:n.699+156_699+157dup
ENST00000617022.4:n.1554-2269_1554-2268dup
ENST00000617847.4:c.952+156_952+157dup
ENST00000620515.1:n.189+156_189+157dup
NM_000107.2:c.1023+156_1023+157dup , LRG_467t1:c.1023+156_1023+157dup NP_000098.1:n.1023+156_1023+157dup
NM_001300734.1:c.457-2269_457-2268dup NP_001287663.1:n.457-2269_457-2268dup
XR_242780.3:n.1013+156_1013+157dup
XR_242780.4:n.1013+156_1013+157dup
NM_000107.3:c.1023+156_1023+157dup MANE Select NP_000098.1:n.1023+156_1023+157dup
NM_001300734.2:c.457-2269_457-2268dup NP_001287663.1:n.457-2269_457-2268dup
NM_001399874.1:c.1023+156_1023+157dup NP_001386803.1:n.1023+156_1023+157dup
NM_001399875.1:c.1023+156_1023+157dup NP_001386804.1:n.1023+156_1023+157dup
NM_001399876.1:c.457-2269_457-2268dup NP_001386805.1:n.457-2269_457-2268dup
NM_001399878.1:c.831+156_831+157dup NP_001386807.1:n.831+156_831+157dup
NR_174610.1:n.1274+156_1274+157dup
NR_174611.1:n.1252+156_1252+157dup