Canonical Allele Identifier: CA2370487946
Gene: DOK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650688T= , CM000682.2:g.54650688T= GRCh38
NC_000020.10:g.53267227T= , CM000682.1:g.53267227T= GRCh37
NC_000020.9:g.52700634T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.*209T= MANE Select ENSP00000262593.5:n.*209T=
ENST00000262593.9:c.*209T= ENSP00000262593.5:n.*209T=
ENST00000395939.5:c.*209T= ENSP00000379270.1:n.*209T=
NM_018431.4:c.*209T= NP_060901.2:n.*209T=
NM_177959.2:c.*209T= NP_808874.1:n.*209T=
XM_011528903.1:c.*209T= XP_011527205.1:n.*209T=
XM_011528904.1:c.*209T= XP_011527206.1:n.*209T=
XM_024451946.1:c.*209T= XP_024307714.1:n.*209T=
NM_018431.5:c.*209T= MANE Select NP_060901.2:n.*209T=
NM_177959.3:c.*209T= NP_808874.1:n.*209T=