Canonical Allele Identifier: CA1616406282
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24347892A= , CM000668.2:g.24347892A= GRCh38
NC_000006.11:g.24348120A= , CM000668.1:g.24348120A= GRCh37
NC_000006.10:g.24456099A= NCBI36
NG_012829.1:g.15161T=
NG_012829.2:g.40401T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.348+5677T= MANE Select ENSP00000367715.3:n.348+5677T=
ENST00000378454.7:c.348+5677T= ENSP00000367715.3:n.348+5677T=
NM_001195610.1:c.348+5677T= NP_001182539.1:n.348+5677T=
NM_016356.4:c.348+5677T= NP_057440.2:n.348+5677T=
NM_016356.5:c.348+5677T= MANE Select NP_057440.2:n.348+5677T=
NM_001195610.2:c.348+5677T= NP_001182539.1:n.348+5677T=