Canonical Allele Identifier: CA1467014827
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030456T= , CM000666.2:g.71030456T= GRCh38
NC_000004.11:g.71896173T= , CM000666.1:g.71896173T= GRCh37
NC_000004.10:g.72115037T= NCBI36
NG_023303.1:g.41909T=

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1078T= MANE Select ENSP00000286648.5:n.*1078T=
ENST00000286648.9:c.*1078T= ENSP00000286648.5:n.*1078T=
ENST00000503359.5:c.*1805T= ENSP00000426389.1:n.*1805T=
ENST00000504730.5:c.*1145T= ENSP00000425578.1:n.*1145T=
ENST00000504952.1:c.*1004T= ENSP00000421508.1:n.*1004T=
NM_000788.2:c.*1078T= NP_000779.1:n.*1078T=
NM_000788.3:c.*1078T= MANE Select NP_000779.1:n.*1078T=