Canonical Allele Identifier: CA2574813996

Gene: DDB2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.47235501_47235503dup , CM000673.2:g.47235501_47235503dup	GRCh38
NC_000011.9:g.47257052_47257054dup , CM000673.1:g.47257052_47257054dup	GRCh37
NC_000011.8:g.47213628_47213630dup	NCBI36
NG_009365.1:g.25560_25562dup , LRG_467:g.25560_25562dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256996.9:c.1023+89_1023+91dup MANE Select	ENSP00000256996.4:n.1023+89_1023+91dup
ENST00000256996.8:c.1023+89_1023+91dup	ENSP00000256996.3:n.1023+89_1023+91dup
ENST00000378600.7:c.457-2336_457-2334dup	ENSP00000367863.3:n.457-2336_457-2334dup
ENST00000378601.7:c.*110+89_*110+91dup	ENSP00000367864.3:n.*110+89_*110+91dup
ENST00000378603.7:c.831+89_831+91dup	ENSP00000367866.3:n.831+89_831+91dup
ENST00000612309.4:n.2472+89_2472+91dup
ENST00000614394.1:n.502_504dup
ENST00000616278.4:c.699+89_699+91dup	ENSP00000478411.1:n.699+89_699+91dup
ENST00000617022.4:n.1554-2336_1554-2334dup
ENST00000617847.4:c.952+89_952+91dup
ENST00000620515.1:n.189+89_189+91dup
NM_000107.2:c.1023+89_1023+91dup , LRG_467t1:c.1023+89_1023+91dup	NP_000098.1:n.1023+89_1023+91dup
NM_001300734.1:c.457-2336_457-2334dup	NP_001287663.1:n.457-2336_457-2334dup
XR_242780.3:n.1013+89_1013+91dup
XR_242780.4:n.1013+89_1013+91dup
NM_000107.3:c.1023+89_1023+91dup MANE Select	NP_000098.1:n.1023+89_1023+91dup
NM_001300734.2:c.457-2336_457-2334dup	NP_001287663.1:n.457-2336_457-2334dup
NM_001399874.1:c.1023+89_1023+91dup	NP_001386803.1:n.1023+89_1023+91dup
NM_001399875.1:c.1023+89_1023+91dup	NP_001386804.1:n.1023+89_1023+91dup
NM_001399876.1:c.457-2336_457-2334dup	NP_001386805.1:n.457-2336_457-2334dup
NM_001399878.1:c.831+89_831+91dup	NP_001386807.1:n.831+89_831+91dup
NR_174610.1:n.1274+89_1274+91dup
NR_174611.1:n.1252+89_1252+91dup