Canonical Allele Identifier: CA99415187
Gene: DCK HGNC NCBI

Linked Data

dbSNP Id: rs1005281576
gnomAD v3: 4-71030382-T-C
gnomAD v4: 4-71030382-T-C
MyVariant Identifiers: chr4:g.71896099T>C (hg19) chr4:g.71030382T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71030382T>C , CM000666.2:g.71030382T>C GRCh38
NC_000004.11:g.71896099T>C , CM000666.1:g.71896099T>C GRCh37
NC_000004.10:g.72114963T>C NCBI36
NG_023303.1:g.41835T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286648.10:c.*1004T>C MANE Select ENSP00000286648.5:n.*1004T>C
ENST00000286648.9:c.*1004T>C ENSP00000286648.5:n.*1004T>C
ENST00000503359.5:c.*1731T>C ENSP00000426389.1:n.*1731T>C
ENST00000504730.5:c.*1071T>C ENSP00000425578.1:n.*1071T>C
ENST00000504952.1:c.*930T>C ENSP00000421508.1:n.*930T>C
NM_000788.2:c.*1004T>C NP_000779.1:n.*1004T>C
NM_000788.3:c.*1004T>C MANE Select NP_000779.1:n.*1004T>C
Search 100 bp 5'
Search 100 bp 3'