Canonical Allele Identifier: CA1969296434
Gene: DDB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47234694_47234695delinsCT , CM000673.2:g.47234694_47234695delinsCT GRCh38
NC_000011.9:g.47256245_47256246delinsCT , CM000673.1:g.47256245_47256246delinsCT GRCh37
NC_000011.8:g.47212821_47212822delinsCT NCBI36
NG_009365.1:g.24753_24754delinsCT , LRG_467:g.24753_24754delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000256996.9:c.702+22_702+23delinsCT MANE Select ENSP00000256996.4:n.702+22_702+23delinsCT...
ENST00000256996.8:c.702+22_702+23delinsCT ENSP00000256996.3:n.702+22_702+23delinsCT...
ENST00000378600.7:c.457-3143_457-3142delinsCT ENSP00000367863.3:n.457-3143_457-3142deli...
ENST00000378601.7:c.702+22_702+23delinsCT ENSP00000367864.3:n.702+22_702+23delinsCT...
ENST00000378603.7:c.510+22_510+23delinsCT ENSP00000367866.3:n.510+22_510+23delinsCT...
ENST00000612309.4:n.1816+22_1816+23delinsCT
ENST00000614394.1:n.92+22_92+23delinsCT
ENST00000616278.4:c.556+22_556+23delinsCT ENSP00000478411.1:n.556+22_556+23delinsCT...
ENST00000617022.4:n.1554-3143_1554-3142delinsCT
ENST00000617847.4:c.631+22_631+23delinsCT
ENST00000620515.1:n.46+22_46+23delinsCT
NM_000107.2:c.702+22_702+23delinsCT , LRG_467t1:c.702+22_702+23delinsCT NP_000098.1:n.702+22_702+23delinsCT
NM_001300734.1:c.457-3143_457-3142delinsCT NP_001287663.1:n.457-3143_457-3142delinsC...
XR_242780.3:n.870+22_870+23delinsCT
XR_242780.4:n.870+22_870+23delinsCT
NM_000107.3:c.702+22_702+23delinsCT MANE Select NP_000098.1:n.702+22_702+23delinsCT
NM_001300734.2:c.457-3143_457-3142delinsCT NP_001287663.1:n.457-3143_457-3142delinsC...
NM_001399874.1:c.702+22_702+23delinsCT NP_001386803.1:n.702+22_702+23delinsCT
NM_001399875.1:c.702+22_702+23delinsCT NP_001386804.1:n.702+22_702+23delinsCT
NM_001399876.1:c.457-3143_457-3142delinsCT NP_001386805.1:n.457-3143_457-3142delinsC...
NM_001399878.1:c.510+22_510+23delinsCT NP_001386807.1:n.510+22_510+23delinsCT
NR_174610.1:n.1131+22_1131+23delinsCT
NR_174611.1:n.989+22_989+23delinsCT