Canonical Allele Identifier: CA1467014888
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030625A= , CM000666.2:g.71030625A= GRCh38
NC_000004.11:g.71896342A= , CM000666.1:g.71896342A= GRCh37
NC_000004.10:g.72115206A= NCBI36
NG_023303.1:g.42078A=

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1247A= MANE Select ENSP00000286648.5:n.*1247A=
ENST00000286648.9:c.*1247A= ENSP00000286648.5:n.*1247A=
ENST00000503359.5:c.*1974A= ENSP00000426389.1:n.*1974A=
ENST00000504730.5:c.*1314A= ENSP00000425578.1:n.*1314A=
ENST00000504952.1:c.*1173A= ENSP00000421508.1:n.*1173A=
NM_000788.2:c.*1247A= NP_000779.1:n.*1247A=
NM_000788.3:c.*1247A= MANE Select NP_000779.1:n.*1247A=