Canonical Allele Identifier: CA2816747377
Gene: DOK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650621del , CM000682.2:g.54650621del GRCh38
NC_000020.10:g.53267160del , CM000682.1:g.53267160del GRCh37
NC_000020.9:g.52700567del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.*142del MANE Select ENSP00000262593.5:n.*142del
ENST00000262593.9:c.*142del ENSP00000262593.5:n.*142del
ENST00000395939.5:c.*142del ENSP00000379270.1:n.*142del
NM_018431.4:c.*142del NP_060901.2:n.*142del
NM_177959.2:c.*142del NP_808874.1:n.*142del
XM_011528903.1:c.*142del XP_011527205.1:n.*142del
XM_011528904.1:c.*142del XP_011527206.1:n.*142del
XM_024451946.1:c.*142del XP_024307714.1:n.*142del
NM_018431.5:c.*142del MANE Select NP_060901.2:n.*142del
NM_177959.3:c.*142del NP_808874.1:n.*142del