Canonical Allele Identifier: CA1616321903
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24174701G= , CM000668.2:g.24174701G= GRCh38
NC_000006.11:g.24174929G= , CM000668.1:g.24174929G= GRCh37
NC_000006.10:g.24282908G= NCBI36
NG_012829.1:g.188352C=
NG_012829.2:g.213592C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.*29C= MANE Select ENSP00000367715.3:n.*29C=
ENST00000378450.6:c.*29C= ENSP00000367711.3:n.*29C=
ENST00000378454.7:c.*29C= ENSP00000367715.3:n.*29C=
NM_001195610.1:c.*29C= NP_001182539.1:n.*29C=
NM_016356.4:c.*29C= NP_057440.2:n.*29C=
NM_016356.5:c.*29C= MANE Select NP_057440.2:n.*29C=
NM_001195610.2:c.*29C= NP_001182539.1:n.*29C=