Canonical Allele Identifier: CA798018762
Gene: DCK HGNC NCBI

Linked Data

dbSNP Id: rs1169470159
MyVariant Identifiers: chr4:g.71896408T>C (hg19) chr4:g.71030691T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030691T>C , CM000666.2:g.71030691T>C GRCh38
NC_000004.11:g.71896408T>C , CM000666.1:g.71896408T>C GRCh37
NC_000004.10:g.72115272T>C NCBI36
NG_023303.1:g.42144T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1313T>C MANE Select ENSP00000286648.5:n.*1313T>C
ENST00000286648.9:c.*1313T>C ENSP00000286648.5:n.*1313T>C
ENST00000503359.5:c.*2040T>C ENSP00000426389.1:n.*2040T>C
ENST00000504730.5:c.*1380T>C ENSP00000425578.1:n.*1380T>C
ENST00000504952.1:c.*1239T>C ENSP00000421508.1:n.*1239T>C
NM_000788.2:c.*1313T>C NP_000779.1:n.*1313T>C
NM_000788.3:c.*1313T>C MANE Select NP_000779.1:n.*1313T>C
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