Canonical Allele Identifier: CA2370487992
Gene: DOK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650798_54650799delinsTG , CM000682.2:g.54650798_54650799delinsTG GRCh38
NC_000020.10:g.53267337_53267338delinsTG , CM000682.1:g.53267337_53267338delinsTG GRCh37
NC_000020.9:g.52700744_52700745delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.*319_*320delinsTG MANE Select ENSP00000262593.5:n.*319_*320delinsTG
ENST00000262593.9:c.*319_*320delinsTG ENSP00000262593.5:n.*319_*320delinsTG
ENST00000395939.5:c.*319_*320delinsTG ENSP00000379270.1:n.*319_*320delinsTG
NM_018431.4:c.*319_*320delinsTG NP_060901.2:n.*319_*320delinsTG
NM_177959.2:c.*319_*320delinsTG NP_808874.1:n.*319_*320delinsTG
XM_011528903.1:c.*319_*320delinsTG XP_011527205.1:n.*319_*320delinsTG
XM_011528904.1:c.*319_*320delinsTG XP_011527206.1:n.*319_*320delinsTG
XM_024451946.1:c.*319_*320delinsTG XP_024307714.1:n.*319_*320delinsTG
NM_018431.5:c.*319_*320delinsTG MANE Select NP_060901.2:n.*319_*320delinsTG
NM_177959.3:c.*319_*320delinsTG NP_808874.1:n.*319_*320delinsTG