Canonical Allele Identifier: CA2762121694
Gene: DCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030675G>A , CM000666.2:g.71030675G>A GRCh38
NC_000004.11:g.71896392G>A , CM000666.1:g.71896392G>A GRCh37
NC_000004.10:g.72115256G>A NCBI36
NG_023303.1:g.42128G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1297G>A MANE Select ENSP00000286648.5:n.*1297G>A
ENST00000286648.9:c.*1297G>A ENSP00000286648.5:n.*1297G>A
ENST00000503359.5:c.*2024G>A ENSP00000426389.1:n.*2024G>A
ENST00000504730.5:c.*1364G>A ENSP00000425578.1:n.*1364G>A
ENST00000504952.1:c.*1223G>A ENSP00000421508.1:n.*1223G>A
NM_000788.2:c.*1297G>A NP_000779.1:n.*1297G>A
NM_000788.3:c.*1297G>A MANE Select NP_000779.1:n.*1297G>A
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