Canonical Allele Identifier: CA1616385263
Gene: DCDC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24205029A= , CM000668.2:g.24205029A= GRCh38
NC_000006.11:g.24205257A= , CM000668.1:g.24205257A= GRCh37
NC_000006.10:g.24313236A= NCBI36
NG_012829.1:g.158024T=
NG_012829.2:g.183264T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.996T= MANE Select ENSP00000367715.3:p.Asp332=
ENST00000378450.6:c.255T= ENSP00000367711.3:p.Asp85=
ENST00000378454.7:c.996T= ENSP00000367715.3:p.Asp332=
NM_001195610.1:c.996T= NP_001182539.1:p.Asp332=
NM_016356.4:c.996T= NP_057440.2:p.Asp332=
NM_016356.5:c.996T= MANE Select NP_057440.2:p.Asp332=
NM_001195610.2:c.996T= NP_001182539.1:p.Asp332=