Canonical Allele Identifier: CA1616385260
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24205026A= , CM000668.2:g.24205026A= GRCh38
NC_000006.11:g.24205254A= , CM000668.1:g.24205254A= GRCh37
NC_000006.10:g.24313233A= NCBI36
NG_012829.1:g.158027T=
NG_012829.2:g.183267T=

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.999T= MANE Select ENSP00000367715.3:p.Thr333=
ENST00000378450.6:c.258T= ENSP00000367711.3:p.Thr86=
ENST00000378454.7:c.999T= ENSP00000367715.3:p.Thr333=
NM_001195610.1:c.999T= NP_001182539.1:p.Thr333=
NM_016356.4:c.999T= NP_057440.2:p.Thr333=
NM_016356.5:c.999T= MANE Select NP_057440.2:p.Thr333=
NM_001195610.2:c.999T= NP_001182539.1:p.Thr333=