Canonical Allele Identifier: CA1616406398
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24347982C= , CM000668.2:g.24347982C= GRCh38
NC_000006.11:g.24348210C= , CM000668.1:g.24348210C= GRCh37
NC_000006.10:g.24456189C= NCBI36
NG_012829.1:g.15071G=
NG_012829.2:g.40311G=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.348+5587G= MANE Select ENSP00000367715.3:n.348+5587G=
ENST00000378454.7:c.348+5587G= ENSP00000367715.3:n.348+5587G=
NM_001195610.1:c.348+5587G= NP_001182539.1:n.348+5587G=
NM_016356.4:c.348+5587G= NP_057440.2:n.348+5587G=
NM_016356.5:c.348+5587G= MANE Select NP_057440.2:n.348+5587G=
NM_001195610.2:c.348+5587G= NP_001182539.1:n.348+5587G=