Canonical Allele Identifier: CA645590545

Gene: DDB2

Linked Data

• COSMIC: COSM4515270

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235404_47235405delinsTT , CM000673.2:g.47235404_47235405delinsTT	GRCh38
NC_000011.9:g.47256955_47256956delinsTT , CM000673.1:g.47256955_47256956delinsTT	GRCh37
NC_000011.8:g.47213531_47213532delinsTT	NCBI36
NG_009365.1:g.25463_25464delinsTT , LRG_467:g.25463_25464delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.1015_1016delinsTT MANE Select	ENSP00000256996.4:p.Pro339Phe
ENST00000256996.8:c.1015_1016delinsTT	ENSP00000256996.3:p.Pro339Phe
ENST00000378600.7:c.457-2433_457-2432delinsTT	ENSP00000367863.3:n.457-2433_457-2432delinsTT
ENST00000378601.7:c.*102_*103delinsTT	ENSP00000367864.3:n.*102_*103delinsTT
ENST00000378603.7:c.823_824delinsTT	ENSP00000367866.3:p.Pro275Phe
ENST00000612309.4:n.2464_2465delinsTT
ENST00000614394.1:n.405_406delinsTT
ENST00000616278.4:c.691_692delinsTT	ENSP00000478411.1:n.691_692delinsTT
ENST00000617022.4:n.1554-2433_1554-2432delinsTT
ENST00000617847.4:c.944_945delinsTT
ENST00000620515.1:n.181_182delinsTT
NM_000107.2:c.1015_1016delinsTT , LRG_467t1:c.1015_1016delinsTT	NP_000098.1:p.Pro339Phe
NM_001300734.1:c.457-2433_457-2432delinsTT	NP_001287663.1:n.457-2433_457-2432delinsTT
XR_242780.3:n.1005_1006delinsTT
XR_242780.4:n.1005_1006delinsTT
NM_000107.3:c.1015_1016delinsTT MANE Select	NP_000098.1:p.Pro339Phe
NM_001300734.2:c.457-2433_457-2432delinsTT	NP_001287663.1:n.457-2433_457-2432delinsTT
NM_001399874.1:c.1015_1016delinsTT	NP_001386803.1:p.Pro339Phe
NM_001399875.1:c.1015_1016delinsTT	NP_001386804.1:p.Pro339Phe
NM_001399876.1:c.457-2433_457-2432delinsTT	NP_001386805.1:n.457-2433_457-2432delinsTT
NM_001399878.1:c.823_824delinsTT	NP_001386807.1:p.Pro275Phe
NR_174610.1:n.1266_1267delinsTT
NR_174611.1:n.1244_1245delinsTT