Canonical Allele Identifier: CA1969296461
Gene: DDB2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.47234713_47234714delinsAC , CM000673.2:g.47234713_47234714delinsAC GRCh38
NC_000011.9:g.47256264_47256265delinsAC , CM000673.1:g.47256264_47256265delinsAC GRCh37
NC_000011.8:g.47212840_47212841delinsAC NCBI36
NG_009365.1:g.24772_24773delinsAC , LRG_467:g.24772_24773delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000256996.9:c.702+41_703-43delinsAC MANE Select ENSP00000256996.4:n.702+41_703-43delinsAC
ENST00000256996.8:c.702+41_703-43delinsAC ENSP00000256996.3:n.702+41_703-43delinsAC
ENST00000378600.7:c.457-3124_457-3123delinsAC ENSP00000367863.3:n.457-3124_457-3123delinsAC
ENST00000378601.7:c.702+41_702+42delinsAC ENSP00000367864.3:n.702+41_702+42delinsAC
ENST00000378603.7:c.510+41_511-43delinsAC ENSP00000367866.3:n.510+41_511-43delinsAC
ENST00000612309.4:n.1816+41_1817-43delinsAC
ENST00000614394.1:n.92+41_93-43delinsAC
ENST00000616278.4:c.556+41_556+42delinsAC ENSP00000478411.1:n.556+41_556+42delinsAC
ENST00000617022.4:n.1554-3124_1554-3123delinsAC
ENST00000617847.4:c.631+41_632-43delinsAC
ENST00000620515.1:n.46+41_46+42delinsAC
NM_000107.2:c.702+41_703-43delinsAC , LRG_467t1:c.702+41_703-43delinsAC NP_000098.1:n.702+41_703-43delinsAC
NM_001300734.1:c.457-3124_457-3123delinsAC NP_001287663.1:n.457-3124_457-3123delinsAC
XR_242780.3:n.870+41_870+42delinsAC
XR_242780.4:n.870+41_870+42delinsAC
NM_000107.3:c.702+41_703-43delinsAC MANE Select NP_000098.1:n.702+41_703-43delinsAC
NM_001300734.2:c.457-3124_457-3123delinsAC NP_001287663.1:n.457-3124_457-3123delinsAC
NM_001399874.1:c.702+41_703-43delinsAC NP_001386803.1:n.702+41_703-43delinsAC
NM_001399875.1:c.702+41_703-43delinsAC NP_001386804.1:n.702+41_703-43delinsAC
NM_001399876.1:c.457-3124_457-3123delinsAC NP_001386805.1:n.457-3124_457-3123delinsAC
NM_001399878.1:c.510+41_511-43delinsAC NP_001386807.1:n.510+41_511-43delinsAC
NR_174610.1:n.1131+41_1131+42delinsAC
NR_174611.1:n.989+41_990-43delinsAC