Canonical Allele Identifier: CA1969297238

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235559_47235561delinsGCT , CM000673.2:g.47235559_47235561delinsGCT	GRCh38
NC_000011.9:g.47257110_47257112delinsGCT , CM000673.1:g.47257110_47257112delinsGCT	GRCh37
NC_000011.8:g.47213686_47213688delinsGCT	NCBI36
NG_009365.1:g.25618_25620delinsGCT , LRG_467:g.25618_25620delinsGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.1023+147_1023+149delinsGCT MANE Select	ENSP00000256996.4:n.1023+147_1023+149delinsGCT
ENST00000256996.8:c.1023+147_1023+149delinsGCT	ENSP00000256996.3:n.1023+147_1023+149delinsGCT
ENST00000378600.7:c.457-2278_457-2276delinsGCT	ENSP00000367863.3:n.457-2278_457-2276delinsGCT
ENST00000378601.7:c.*110+147_*110+149delinsGCT	ENSP00000367864.3:n.*110+147_*110+149delinsGCT
ENST00000378603.7:c.831+147_831+149delinsGCT	ENSP00000367866.3:n.831+147_831+149delinsGCT
ENST00000612309.4:n.2472+147_2472+149delinsGCT
ENST00000614394.1:n.560_562delinsGCT
ENST00000616278.4:c.699+147_699+149delinsGCT	ENSP00000478411.1:n.699+147_699+149delinsGCT
ENST00000617022.4:n.1554-2278_1554-2276delinsGCT
ENST00000617847.4:c.952+147_952+149delinsGCT
ENST00000620515.1:n.189+147_189+149delinsGCT
NM_000107.2:c.1023+147_1023+149delinsGCT , LRG_467t1:c.1023+147_1023+149delinsGCT	NP_000098.1:n.1023+147_1023+149delinsGCT
NM_001300734.1:c.457-2278_457-2276delinsGCT	NP_001287663.1:n.457-2278_457-2276delinsGCT
XR_242780.3:n.1013+147_1013+149delinsGCT
XR_242780.4:n.1013+147_1013+149delinsGCT
NM_000107.3:c.1023+147_1023+149delinsGCT MANE Select	NP_000098.1:n.1023+147_1023+149delinsGCT
NM_001300734.2:c.457-2278_457-2276delinsGCT	NP_001287663.1:n.457-2278_457-2276delinsGCT
NM_001399874.1:c.1023+147_1023+149delinsGCT	NP_001386803.1:n.1023+147_1023+149delinsGCT
NM_001399875.1:c.1023+147_1023+149delinsGCT	NP_001386804.1:n.1023+147_1023+149delinsGCT
NM_001399876.1:c.457-2278_457-2276delinsGCT	NP_001386805.1:n.457-2278_457-2276delinsGCT
NM_001399878.1:c.831+147_831+149delinsGCT	NP_001386807.1:n.831+147_831+149delinsGCT
NR_174610.1:n.1274+147_1274+149delinsGCT
NR_174611.1:n.1252+147_1252+149delinsGCT