Canonical Allele Identifier: CA1616325771
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178419C= , CM000668.2:g.24178419C= GRCh38
NC_000006.11:g.24178647C= , CM000668.1:g.24178647C= GRCh37
NC_000006.10:g.24286626C= NCBI36
NG_012829.1:g.184634G=
NG_012829.2:g.209874G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1237G= MANE Select ENSP00000367715.3:p.Gly413=
ENST00000378450.6:c.496G= ENSP00000367711.3:p.Gly166=
ENST00000378454.7:c.1237G= ENSP00000367715.3:p.Gly413=
NM_001195610.1:c.1237G= NP_001182539.1:p.Gly413=
NM_016356.4:c.1237G= NP_057440.2:p.Gly413=
NM_016356.5:c.1237G= MANE Select NP_057440.2:p.Gly413=
NM_001195610.2:c.1237G= NP_001182539.1:p.Gly413=