Canonical Allele Identifier: CA745650000
Gene: DOK5 HGNC NCBI

Linked Data

dbSNP Id: rs1242716983
MyVariant Identifiers: chr20:g.53267144G>A (hg19) chr20:g.54650605G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650605G>A , CM000682.2:g.54650605G>A GRCh38
NC_000020.10:g.53267144G>A , CM000682.1:g.53267144G>A GRCh37
NC_000020.9:g.52700551G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262593.10:c.*126G>A MANE Select ENSP00000262593.5:n.*126G>A
ENST00000262593.9:c.*126G>A ENSP00000262593.5:n.*126G>A
ENST00000395939.5:c.*126G>A ENSP00000379270.1:n.*126G>A
NM_018431.4:c.*126G>A NP_060901.2:n.*126G>A
NM_177959.2:c.*126G>A NP_808874.1:n.*126G>A
XM_011528903.1:c.*126G>A XP_011527205.1:n.*126G>A
XM_011528904.1:c.*126G>A XP_011527206.1:n.*126G>A
XM_024451946.1:c.*126G>A XP_024307714.1:n.*126G>A
NM_018431.5:c.*126G>A MANE Select NP_060901.2:n.*126G>A
NM_177959.3:c.*126G>A NP_808874.1:n.*126G>A
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