Canonical Allele Identifier: CA2762121690
Gene: DCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030549del , CM000666.2:g.71030549del GRCh38
NC_000004.11:g.71896266del , CM000666.1:g.71896266del GRCh37
NC_000004.10:g.72115130del NCBI36
NG_023303.1:g.42002del

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1171del MANE Select ENSP00000286648.5:n.*1171del
ENST00000286648.9:c.*1171del ENSP00000286648.5:n.*1171del
ENST00000503359.5:c.*1898del ENSP00000426389.1:n.*1898del
ENST00000504730.5:c.*1238del ENSP00000425578.1:n.*1238del
ENST00000504952.1:c.*1097del ENSP00000421508.1:n.*1097del
NM_000788.2:c.*1171del NP_000779.1:n.*1171del
NM_000788.3:c.*1171del MANE Select NP_000779.1:n.*1171del