Canonical Allele Identifier: CA2370487828
Gene: DOK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650398A= , CM000682.2:g.54650398A= GRCh38
NC_000020.10:g.53266937A= , CM000682.1:g.53266937A= GRCh37
NC_000020.9:g.52700344A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.857-17A= MANE Select ENSP00000262593.5:n.857-17A=
ENST00000262593.9:c.857-17A= ENSP00000262593.5:n.857-17A=
ENST00000395939.5:c.533-17A= ENSP00000379270.1:n.533-17A=
NM_018431.4:c.857-17A= NP_060901.2:n.857-17A=
NM_177959.2:c.533-17A= NP_808874.1:n.533-17A=
XM_011528903.1:c.821-17A= XP_011527205.1:n.821-17A=
XM_011528904.1:c.533-17A= XP_011527206.1:n.533-17A=
XM_024451946.1:c.821-17A= XP_024307714.1:n.821-17A=
NM_018431.5:c.857-17A= MANE Select NP_060901.2:n.857-17A=
NM_177959.3:c.533-17A= NP_808874.1:n.533-17A=