Canonical Allele Identifier: CA2574813987

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235378del , CM000673.2:g.47235378del	GRCh38
NC_000011.9:g.47256929del , CM000673.1:g.47256929del	GRCh37
NC_000011.8:g.47213505del	NCBI36
NG_009365.1:g.25437del , LRG_467:g.25437del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.989del MANE Select	ENSP00000256996.4:p.Pro330LeufsTer?
ENST00000256996.8:c.989del	ENSP00000256996.3:p.Pro330LeufsTer?
ENST00000378600.7:c.457-2459del	ENSP00000367863.3:n.457-2459del
ENST00000378601.7:c.*76del	ENSP00000367864.3:n.*76del
ENST00000378603.7:c.797del	ENSP00000367866.3:p.Pro266LeufsTer?
ENST00000612309.4:n.2438del
ENST00000614394.1:n.379del
ENST00000616278.4:c.665del	ENSP00000478411.1:n.665del
ENST00000617022.4:n.1554-2459del
ENST00000617847.4:c.918del
ENST00000620515.1:n.155del
NM_000107.2:c.989del , LRG_467t1:c.989del	NP_000098.1:p.Pro330LeufsTer?
NM_001300734.1:c.457-2459del	NP_001287663.1:n.457-2459del
XR_242780.3:n.979del
XR_242780.4:n.979del
NM_000107.3:c.989del MANE Select	NP_000098.1:p.Pro330LeufsTer?
NM_001300734.2:c.457-2459del	NP_001287663.1:n.457-2459del
NM_001399874.1:c.989del	NP_001386803.1:p.Pro330LeufsTer?
NM_001399875.1:c.989del	NP_001386804.1:p.Pro330LeufsTer?
NM_001399876.1:c.457-2459del	NP_001386805.1:n.457-2459del
NM_001399878.1:c.797del	NP_001386807.1:p.Pro266LeufsTer?
NR_174610.1:n.1240del
NR_174611.1:n.1218del