Canonical Allele Identifier: CA745650026
Gene: DOK5 HGNC NCBI

Linked Data

dbSNP Id: rs1410175343
gnomAD v3: 20-54650677-T-C
gnomAD v4: 20-54650677-T-C
MyVariant Identifiers: chr20:g.53267216T>C (hg19) chr20:g.54650677T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650677T>C , CM000682.2:g.54650677T>C GRCh38
NC_000020.10:g.53267216T>C , CM000682.1:g.53267216T>C GRCh37
NC_000020.9:g.52700623T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.*198T>C MANE Select ENSP00000262593.5:n.*198T>C
ENST00000262593.9:c.*198T>C ENSP00000262593.5:n.*198T>C
ENST00000395939.5:c.*198T>C ENSP00000379270.1:n.*198T>C
NM_018431.4:c.*198T>C NP_060901.2:n.*198T>C
NM_177959.2:c.*198T>C NP_808874.1:n.*198T>C
XM_011528903.1:c.*198T>C XP_011527205.1:n.*198T>C
XM_011528904.1:c.*198T>C XP_011527206.1:n.*198T>C
XM_024451946.1:c.*198T>C XP_024307714.1:n.*198T>C
NM_018431.5:c.*198T>C MANE Select NP_060901.2:n.*198T>C
NM_177959.3:c.*198T>C NP_808874.1:n.*198T>C
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