Canonical Allele Identifier: CA1467014824
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030442G= , CM000666.2:g.71030442G= GRCh38
NC_000004.11:g.71896159G= , CM000666.1:g.71896159G= GRCh37
NC_000004.10:g.72115023G= NCBI36
NG_023303.1:g.41895G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1064G= MANE Select ENSP00000286648.5:n.*1064G=
ENST00000286648.9:c.*1064G= ENSP00000286648.5:n.*1064G=
ENST00000503359.5:c.*1791G= ENSP00000426389.1:n.*1791G=
ENST00000504730.5:c.*1131G= ENSP00000425578.1:n.*1131G=
ENST00000504952.1:c.*990G= ENSP00000421508.1:n.*990G=
NM_000788.2:c.*1064G= NP_000779.1:n.*1064G=
NM_000788.3:c.*1064G= MANE Select NP_000779.1:n.*1064G=