Canonical Allele Identifier: CA2613377967

Gene: DDB2

Linked Data

• gnomAD v4: 11-47235111-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235118del , CM000673.2:g.47235118del	GRCh38
NC_000011.9:g.47256669del , CM000673.1:g.47256669del	GRCh37
NC_000011.8:g.47213245del	NCBI36
NG_009365.1:g.25177del , LRG_467:g.25177del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.881-152del MANE Select	ENSP00000256996.4:n.881-152del
ENST00000256996.8:c.881-152del	ENSP00000256996.3:n.881-152del
ENST00000378600.7:c.457-2719del	ENSP00000367863.3:n.457-2719del
ENST00000378601.7:c.703-152del	ENSP00000367864.3:n.703-152del
ENST00000378603.7:c.689-152del	ENSP00000367866.3:n.689-152del
ENST00000612309.4:n.2178del
ENST00000614394.1:n.271-152del
ENST00000616278.4:c.557-152del	ENSP00000478411.1:n.557-152del
ENST00000617022.4:n.1554-2719del
ENST00000617847.4:c.810-152del
ENST00000620515.1:n.47-152del
NM_000107.2:c.881-152del , LRG_467t1:c.881-152del	NP_000098.1:n.881-152del
NM_001300734.1:c.457-2719del	NP_001287663.1:n.457-2719del
XR_242780.3:n.871-152del
XR_242780.4:n.871-152del
NM_000107.3:c.881-152del MANE Select	NP_000098.1:n.881-152del
NM_001300734.2:c.457-2719del	NP_001287663.1:n.457-2719del
NM_001399874.1:c.881-152del	NP_001386803.1:n.881-152del
NM_001399875.1:c.881-152del	NP_001386804.1:n.881-152del
NM_001399876.1:c.457-2719del	NP_001386805.1:n.457-2719del
NM_001399878.1:c.689-152del	NP_001386807.1:n.689-152del
NR_174610.1:n.1132-152del
NR_174611.1:n.1110-152del