Canonical Allele Identifier: CA363279768

Gene: DCDC2

Linked Data

• COSMIC: COSM741011 ; COSM4861775
• MyVariant Identifiers: chr6:g.24178600G>T (hg19) ; chr6:g.24178372G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24178372G>T , CM000668.2:g.24178372G>T	GRCh38
NC_000006.11:g.24178600G>T , CM000668.1:g.24178600G>T	GRCh37
NC_000006.10:g.24286579G>T	NCBI36
NG_012829.1:g.184681C>A
NG_012829.2:g.209921C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1284C>A MANE Select	ENSP00000367715.3:p.Asp428Glu
ENST00000378450.6:c.543C>A	ENSP00000367711.3:p.Asp181Glu
ENST00000378454.7:c.1284C>A	ENSP00000367715.3:p.Asp428Glu
NM_001195610.1:c.1284C>A	NP_001182539.1:p.Asp428Glu
NM_016356.4:c.1284C>A	NP_057440.2:p.Asp428Glu
NM_016356.5:c.1284C>A MANE Select	NP_057440.2:p.Asp428Glu
NM_001195610.2:c.1284C>A	NP_001182539.1:p.Asp428Glu