Canonical Allele Identifier: CA136636006
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs149729223

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24290788del , CM000668.2:g.24290788del GRCh38
NC_000006.11:g.24291016del , CM000668.1:g.24291016del GRCh37
NC_000006.10:g.24398995del NCBI36
NG_012829.1:g.72265del
NG_012829.2:g.97505del

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.704+144del MANE Select ENSP00000367715.3:n.704+144del
ENST00000378454.7:c.704+144del ENSP00000367715.3:n.704+144del
NM_001195610.1:c.704+144del NP_001182539.1:n.704+144del
NM_016356.4:c.704+144del NP_057440.2:n.704+144del
NM_016356.5:c.704+144del MANE Select NP_057440.2:n.704+144del
NM_001195610.2:c.704+144del NP_001182539.1:n.704+144del