Canonical Allele Identifier: CA552436423
Gene: DCK HGNC NCBI

Linked Data

dbSNP Id: rs1315085573
gnomAD v2: 4-71896151-C-G
gnomAD v3: 4-71030434-C-G
gnomAD v4: 4-71030434-C-G
MyVariant Identifiers: chr4:g.71896151C>G (hg19) chr4:g.71030434C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030434C>G , CM000666.2:g.71030434C>G GRCh38
NC_000004.11:g.71896151C>G , CM000666.1:g.71896151C>G GRCh37
NC_000004.10:g.72115015C>G NCBI36
NG_023303.1:g.41887C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1056C>G MANE Select ENSP00000286648.5:n.*1056C>G
ENST00000286648.9:c.*1056C>G ENSP00000286648.5:n.*1056C>G
ENST00000503359.5:c.*1783C>G ENSP00000426389.1:n.*1783C>G
ENST00000504730.5:c.*1123C>G ENSP00000425578.1:n.*1123C>G
ENST00000504952.1:c.*982C>G ENSP00000421508.1:n.*982C>G
NM_000788.2:c.*1056C>G NP_000779.1:n.*1056C>G
NM_000788.3:c.*1056C>G MANE Select NP_000779.1:n.*1056C>G
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