Canonical Allele Identifier: CA1086921871
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1760966911

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178117_24178149del , CM000668.2:g.24178117_24178149del GRCh38
NC_000006.11:g.24178345_24178377del , CM000668.1:g.24178345_24178377del GRCh37
NC_000006.10:g.24286324_24286356del NCBI36
NG_012829.1:g.184912_184944del
NG_012829.2:g.210152_210184del

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1326+189_1326+221del MANE Select ENSP00000367715.3:n.1326+189_1326+221del
ENST00000378450.6:c.585+189_585+221del ENSP00000367711.3:n.585+189_585+221del
ENST00000378454.7:c.1326+189_1326+221del ENSP00000367715.3:n.1326+189_1326+221del
NM_001195610.1:c.1326+189_1326+221del NP_001182539.1:n.1326+189_1326+221del
NM_016356.4:c.1326+189_1326+221del NP_057440.2:n.1326+189_1326+221del
NM_016356.5:c.1326+189_1326+221del MANE Select NP_057440.2:n.1326+189_1326+221del
NM_001195610.2:c.1326+189_1326+221del NP_001182539.1:n.1326+189_1326+221del