Canonical Allele Identifier: CA2762121692
Gene: DCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030649T>A , CM000666.2:g.71030649T>A GRCh38
NC_000004.11:g.71896366T>A , CM000666.1:g.71896366T>A GRCh37
NC_000004.10:g.72115230T>A NCBI36
NG_023303.1:g.42102T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1271T>A MANE Select ENSP00000286648.5:n.*1271T>A
ENST00000286648.9:c.*1271T>A ENSP00000286648.5:n.*1271T>A
ENST00000503359.5:c.*1998T>A ENSP00000426389.1:n.*1998T>A
ENST00000504730.5:c.*1338T>A ENSP00000425578.1:n.*1338T>A
ENST00000504952.1:c.*1197T>A ENSP00000421508.1:n.*1197T>A
NM_000788.2:c.*1271T>A NP_000779.1:n.*1271T>A
NM_000788.3:c.*1271T>A MANE Select NP_000779.1:n.*1271T>A
Search 100 bp 5'
Search 100 bp 3'