Canonical Allele Identifier: CA363279631
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs751396384
gnomAD v4: 6-24178338-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178338G>T , CM000668.2:g.24178338G>T GRCh38
NC_000006.11:g.24178566G>T , CM000668.1:g.24178566G>T GRCh37
NC_000006.10:g.24286545G>T NCBI36
NG_012829.1:g.184715C>A
NG_012829.2:g.209955C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1318C>A MANE Select ENSP00000367715.3:p.Gln440Lys
ENST00000378450.6:c.577C>A ENSP00000367711.3:p.Gln193Lys
ENST00000378454.7:c.1318C>A ENSP00000367715.3:p.Gln440Lys
NM_001195610.1:c.1318C>A NP_001182539.1:p.Gln440Lys
NM_016356.4:c.1318C>A NP_057440.2:p.Gln440Lys
NM_016356.5:c.1318C>A MANE Select NP_057440.2:p.Gln440Lys
NM_001195610.2:c.1318C>A NP_001182539.1:p.Gln440Lys