Canonical Allele Identifier: CA2370487903
Gene: DOK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650587A= , CM000682.2:g.54650587A= GRCh38
NC_000020.10:g.53267126A= , CM000682.1:g.53267126A= GRCh37
NC_000020.9:g.52700533A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.*108A= MANE Select ENSP00000262593.5:n.*108A=
ENST00000262593.9:c.*108A= ENSP00000262593.5:n.*108A=
ENST00000395939.5:c.*108A= ENSP00000379270.1:n.*108A=
NM_018431.4:c.*108A= NP_060901.2:n.*108A=
NM_177959.2:c.*108A= NP_808874.1:n.*108A=
XM_011528903.1:c.*108A= XP_011527205.1:n.*108A=
XM_011528904.1:c.*108A= XP_011527206.1:n.*108A=
XM_024451946.1:c.*108A= XP_024307714.1:n.*108A=
NM_018431.5:c.*108A= MANE Select NP_060901.2:n.*108A=
NM_177959.3:c.*108A= NP_808874.1:n.*108A=