Canonical Allele Identifier: CA2816747387
Gene: DOK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650762A>T , CM000682.2:g.54650762A>T GRCh38
NC_000020.10:g.53267301A>T , CM000682.1:g.53267301A>T GRCh37
NC_000020.9:g.52700708A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.*283A>T MANE Select ENSP00000262593.5:n.*283A>T
ENST00000262593.9:c.*283A>T ENSP00000262593.5:n.*283A>T
ENST00000395939.5:c.*283A>T ENSP00000379270.1:n.*283A>T
NM_018431.4:c.*283A>T NP_060901.2:n.*283A>T
NM_177959.2:c.*283A>T NP_808874.1:n.*283A>T
XM_011528903.1:c.*283A>T XP_011527205.1:n.*283A>T
XM_011528904.1:c.*283A>T XP_011527206.1:n.*283A>T
XM_024451946.1:c.*283A>T XP_024307714.1:n.*283A>T
NM_018431.5:c.*283A>T MANE Select NP_060901.2:n.*283A>T
NM_177959.3:c.*283A>T NP_808874.1:n.*283A>T