Canonical Allele Identifier: CA363279948

Gene: DCDC2

Linked Data

• gnomAD v4: 6-24178423-C-G
• MyVariant Identifiers: chr6:g.24178651C>G (hg19) ; chr6:g.24178423C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.24178423C>G , CM000668.2:g.24178423C>G	GRCh38
NC_000006.11:g.24178651C>G , CM000668.1:g.24178651C>G	GRCh37
NC_000006.10:g.24286630C>G	NCBI36
NG_012829.1:g.184630G>C
NG_012829.2:g.209870G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378454.8:c.1233G>C MANE Select	ENSP00000367715.3:p.Glu411Asp
ENST00000378450.6:c.492G>C	ENSP00000367711.3:p.Glu164Asp
ENST00000378454.7:c.1233G>C	ENSP00000367715.3:p.Glu411Asp
NM_001195610.1:c.1233G>C	NP_001182539.1:p.Glu411Asp
NM_016356.4:c.1233G>C	NP_057440.2:p.Glu411Asp
NM_016356.5:c.1233G>C MANE Select	NP_057440.2:p.Glu411Asp
NM_001195610.2:c.1233G>C	NP_001182539.1:p.Glu411Asp