Canonical Allele Identifier: CA2370487899
Gene: DOK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650581A= , CM000682.2:g.54650581A= GRCh38
NC_000020.10:g.53267120A= , CM000682.1:g.53267120A= GRCh37
NC_000020.9:g.52700527A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262593.10:c.*102A= MANE Select ENSP00000262593.5:n.*102A=
ENST00000262593.9:c.*102A= ENSP00000262593.5:n.*102A=
ENST00000395939.5:c.*102A= ENSP00000379270.1:n.*102A=
NM_018431.4:c.*102A= NP_060901.2:n.*102A=
NM_177959.2:c.*102A= NP_808874.1:n.*102A=
XM_011528903.1:c.*102A= XP_011527205.1:n.*102A=
XM_011528904.1:c.*102A= XP_011527206.1:n.*102A=
XM_024451946.1:c.*102A= XP_024307714.1:n.*102A=
NM_018431.5:c.*102A= MANE Select NP_060901.2:n.*102A=
NM_177959.3:c.*102A= NP_808874.1:n.*102A=