Canonical Allele Identifier: CA1616420477
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24273495A= , CM000668.2:g.24273495A= GRCh38
NC_000006.11:g.24273723A= , CM000668.1:g.24273723A= GRCh37
NC_000006.10:g.24381702A= NCBI36
NG_012829.1:g.89558T=
NG_012829.2:g.114798T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.922+4554T= MANE Select ENSP00000367715.3:n.922+4554T=
ENST00000378454.7:c.922+4554T= ENSP00000367715.3:n.922+4554T=
NM_001195610.1:c.922+4554T= NP_001182539.1:n.922+4554T=
NM_016356.4:c.922+4554T= NP_057440.2:n.922+4554T=
NM_016356.5:c.922+4554T= MANE Select NP_057440.2:n.922+4554T=
NM_001195610.2:c.922+4554T= NP_001182539.1:n.922+4554T=