Canonical Allele Identifier: CA363280319
Gene: DCDC2 HGNC NCBI

Linked Data

COSMIC: COSM3860717 COSM3860718
MyVariant Identifiers: chr6:g.24178723T>G (hg19) chr6:g.24178495T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.24178495T>G , CM000668.2:g.24178495T>G GRCh38
NC_000006.11:g.24178723T>G , CM000668.1:g.24178723T>G GRCh37
NC_000006.10:g.24286702T>G NCBI36
NG_012829.1:g.184558A>C
NG_012829.2:g.209798A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000378454.8:c.1161A>C MANE Select ENSP00000367715.3:p.Gln387His
ENST00000378450.6:c.420A>C ENSP00000367711.3:p.Gln140His
ENST00000378454.7:c.1161A>C ENSP00000367715.3:p.Gln387His
NM_001195610.1:c.1161A>C NP_001182539.1:p.Gln387His
NM_016356.4:c.1161A>C NP_057440.2:p.Gln387His
NM_016356.5:c.1161A>C MANE Select NP_057440.2:p.Gln387His
NM_001195610.2:c.1161A>C NP_001182539.1:p.Gln387His
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