Canonical Allele Identifier: CA552436447
Gene: DCK HGNC NCBI

Linked Data

dbSNP Id: rs1432540468
gnomAD v2: 4-71896419-G-GT
gnomAD v3: 4-71030702-G-GT
gnomAD v4: 4-71030702-G-GT
MyVariant Identifiers: chr4:g.71896419_71896420insT (hg19) chr4:g.71030702_71030703insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030703dup , CM000666.2:g.71030703dup GRCh38
NC_000004.11:g.71896420dup , CM000666.1:g.71896420dup GRCh37
NC_000004.10:g.72115284dup NCBI36
NG_023303.1:g.42156dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1325dup MANE Select ENSP00000286648.5:n.*1325dup
ENST00000286648.9:c.*1325dup ENSP00000286648.5:n.*1325dup
ENST00000503359.5:c.*2052dup ENSP00000426389.1:n.*2052dup
ENST00000504730.5:c.*1392dup ENSP00000425578.1:n.*1392dup
ENST00000504952.1:c.*1251dup ENSP00000421508.1:n.*1251dup
NM_000788.2:c.*1325dup NP_000779.1:n.*1325dup
NM_000788.3:c.*1325dup MANE Select NP_000779.1:n.*1325dup
Search 100 bp 5'
Search 100 bp 3'