Canonical Allele Identifier: CA1467014811
Gene: DCK HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030414A= , CM000666.2:g.71030414A= GRCh38
NC_000004.11:g.71896131A= , CM000666.1:g.71896131A= GRCh37
NC_000004.10:g.72114995A= NCBI36
NG_023303.1:g.41867A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1036A= MANE Select ENSP00000286648.5:n.*1036A=
ENST00000286648.9:c.*1036A= ENSP00000286648.5:n.*1036A=
ENST00000503359.5:c.*1763A= ENSP00000426389.1:n.*1763A=
ENST00000504730.5:c.*1103A= ENSP00000425578.1:n.*1103A=
ENST00000504952.1:c.*962A= ENSP00000421508.1:n.*962A=
NM_000788.2:c.*1036A= NP_000779.1:n.*1036A=
NM_000788.3:c.*1036A= MANE Select NP_000779.1:n.*1036A=
Search 100 bp 5'
Search 100 bp 3'