Canonical Allele Identifier: CA363279744
Gene: DCDC2 HGNC NCBI

Linked Data

dbSNP Id: rs1161113374

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178367T>A , CM000668.2:g.24178367T>A GRCh38
NC_000006.11:g.24178595T>A , CM000668.1:g.24178595T>A GRCh37
NC_000006.10:g.24286574T>A NCBI36
NG_012829.1:g.184686A>T
NG_012829.2:g.209926A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000378454.8:c.1289A>T MANE Select ENSP00000367715.3:p.Glu430Val
ENST00000378450.6:c.548A>T ENSP00000367711.3:p.Glu183Val
ENST00000378454.7:c.1289A>T ENSP00000367715.3:p.Glu430Val
NM_001195610.1:c.1289A>T NP_001182539.1:p.Glu430Val
NM_016356.4:c.1289A>T NP_057440.2:p.Glu430Val
NM_016356.5:c.1289A>T MANE Select NP_057440.2:p.Glu430Val
NM_001195610.2:c.1289A>T NP_001182539.1:p.Glu430Val