Canonical Allele Identifier: CA2816747381
Gene: DOK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650674_54650675insTA , CM000682.2:g.54650674_54650675insTA GRCh38
NC_000020.10:g.53267213_53267214insTA , CM000682.1:g.53267213_53267214insTA GRCh37
NC_000020.9:g.52700620_52700621insTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.*195_*196insTA MANE Select ENSP00000262593.5:n.*195_*196insTA
ENST00000262593.9:c.*195_*196insTA ENSP00000262593.5:n.*195_*196insTA
ENST00000395939.5:c.*195_*196insTA ENSP00000379270.1:n.*195_*196insTA
NM_018431.4:c.*195_*196insTA NP_060901.2:n.*195_*196insTA
NM_177959.2:c.*195_*196insTA NP_808874.1:n.*195_*196insTA
XM_011528903.1:c.*195_*196insTA XP_011527205.1:n.*195_*196insTA
XM_011528904.1:c.*195_*196insTA XP_011527206.1:n.*195_*196insTA
XM_024451946.1:c.*195_*196insTA XP_024307714.1:n.*195_*196insTA
NM_018431.5:c.*195_*196insTA MANE Select NP_060901.2:n.*195_*196insTA
NM_177959.3:c.*195_*196insTA NP_808874.1:n.*195_*196insTA