Canonical Allele Identifier: CA2370488020
Gene: DOK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650864A= , CM000682.2:g.54650864A= GRCh38
NC_000020.10:g.53267403A= , CM000682.1:g.53267403A= GRCh37
NC_000020.9:g.52700810A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.*385A= MANE Select ENSP00000262593.5:n.*385A=
ENST00000262593.9:c.*385A= ENSP00000262593.5:n.*385A=
ENST00000395939.5:c.*385A= ENSP00000379270.1:n.*385A=
NM_018431.4:c.*385A= NP_060901.2:n.*385A=
NM_177959.2:c.*385A= NP_808874.1:n.*385A=
XM_011528903.1:c.*385A= XP_011527205.1:n.*385A=
XM_011528904.1:c.*385A= XP_011527206.1:n.*385A=
XM_024451946.1:c.*385A= XP_024307714.1:n.*385A=
NM_018431.5:c.*385A= MANE Select NP_060901.2:n.*385A=
NM_177959.3:c.*385A= NP_808874.1:n.*385A=