Canonical Allele Identifier: CA1616385130
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1761670212

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24204701del , CM000668.2:g.24204701del GRCh38
NC_000006.11:g.24204929del , CM000668.1:g.24204929del GRCh37
NC_000006.10:g.24312908del NCBI36
NG_012829.1:g.158357del
NG_012829.2:g.183597del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1023+306del MANE Select ENSP00000367715.3:n.1023+306del
ENST00000378450.6:c.282+306del ENSP00000367711.3:n.282+306del
ENST00000378454.7:c.1023+306del ENSP00000367715.3:n.1023+306del
NM_001195610.1:c.1023+306del NP_001182539.1:n.1023+306del
NM_016356.4:c.1023+306del NP_057440.2:n.1023+306del
NM_016356.5:c.1023+306del MANE Select NP_057440.2:n.1023+306del
NM_001195610.2:c.1023+306del NP_001182539.1:n.1023+306del