Canonical Allele Identifier: CA1969297230

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235551A= , CM000673.2:g.47235551A=	GRCh38
NC_000011.9:g.47257102A= , CM000673.1:g.47257102A=	GRCh37
NC_000011.8:g.47213678A=	NCBI36
NG_009365.1:g.25610A= , LRG_467:g.25610A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.1023+139A= MANE Select	ENSP00000256996.4:n.1023+139A=
ENST00000256996.8:c.1023+139A=	ENSP00000256996.3:n.1023+139A=
ENST00000378600.7:c.457-2286A=	ENSP00000367863.3:n.457-2286A=
ENST00000378601.7:c.*110+139A=	ENSP00000367864.3:n.*110+139A=
ENST00000378603.7:c.831+139A=	ENSP00000367866.3:n.831+139A=
ENST00000612309.4:n.2472+139A=
ENST00000614394.1:n.552A=
ENST00000616278.4:c.699+139A=	ENSP00000478411.1:n.699+139A=
ENST00000617022.4:n.1554-2286A=
ENST00000617847.4:c.952+139A=
ENST00000620515.1:n.189+139A=
NM_000107.2:c.1023+139A= , LRG_467t1:c.1023+139A=	NP_000098.1:n.1023+139A=
NM_001300734.1:c.457-2286A=	NP_001287663.1:n.457-2286A=
XR_242780.3:n.1013+139A=
XR_242780.4:n.1013+139A=
NM_000107.3:c.1023+139A= MANE Select	NP_000098.1:n.1023+139A=
NM_001300734.2:c.457-2286A=	NP_001287663.1:n.457-2286A=
NM_001399874.1:c.1023+139A=	NP_001386803.1:n.1023+139A=
NM_001399875.1:c.1023+139A=	NP_001386804.1:n.1023+139A=
NM_001399876.1:c.457-2286A=	NP_001386805.1:n.457-2286A=
NM_001399878.1:c.831+139A=	NP_001386807.1:n.831+139A=
NR_174610.1:n.1274+139A=
NR_174611.1:n.1252+139A=