Canonical Allele Identifier: CA2670931580
Gene: DCK HGNC NCBI

Linked Data

gnomAD v4: 4-71030613-AT-A
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030616del , CM000666.2:g.71030616del GRCh38
NC_000004.11:g.71896333del , CM000666.1:g.71896333del GRCh37
NC_000004.10:g.72115197del NCBI36
NG_023303.1:g.42069del

Transcript Alleles

HGVS Amino-acid change
ENST00000286648.10:c.*1238del MANE Select ENSP00000286648.5:n.*1238del
ENST00000286648.9:c.*1238del ENSP00000286648.5:n.*1238del
ENST00000503359.5:c.*1965del ENSP00000426389.1:n.*1965del
ENST00000504730.5:c.*1305del ENSP00000425578.1:n.*1305del
ENST00000504952.1:c.*1164del ENSP00000421508.1:n.*1164del
NM_000788.2:c.*1238del NP_000779.1:n.*1238del
NM_000788.3:c.*1238del MANE Select NP_000779.1:n.*1238del
Search 100 bp 5'
Search 100 bp 3'