Canonical Allele Identifier: CA2370488013
Gene: DOK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650849_54650853delinsACAGT , CM000682.2:g.54650849_54650853delinsACAGT GRCh38
NC_000020.10:g.53267388_53267392delinsACAGT , CM000682.1:g.53267388_53267392delinsACAGT GRCh37
NC_000020.9:g.52700795_52700799delinsACAGT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.*370_*374delinsACAGT MANE Select ENSP00000262593.5:n.*370_*374delinsACAGT
ENST00000262593.9:c.*370_*374delinsACAGT ENSP00000262593.5:n.*370_*374delinsACAGT
ENST00000395939.5:c.*370_*374delinsACAGT ENSP00000379270.1:n.*370_*374delinsACAGT
NM_018431.4:c.*370_*374delinsACAGT NP_060901.2:n.*370_*374delinsACAGT
NM_177959.2:c.*370_*374delinsACAGT NP_808874.1:n.*370_*374delinsACAGT
XM_011528903.1:c.*370_*374delinsACAGT XP_011527205.1:n.*370_*374delinsACAGT
XM_011528904.1:c.*370_*374delinsACAGT XP_011527206.1:n.*370_*374delinsACAGT
XM_024451946.1:c.*370_*374delinsACAGT XP_024307714.1:n.*370_*374delinsACAGT
NM_018431.5:c.*370_*374delinsACAGT MANE Select NP_060901.2:n.*370_*374delinsACAGT
NM_177959.3:c.*370_*374delinsACAGT NP_808874.1:n.*370_*374delinsACAGT