Canonical Allele Identifier: CA2370488003

Gene: DOK5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54650822_54650826delinsTTTCC , CM000682.2:g.54650822_54650826delinsTTTCC	GRCh38
NC_000020.10:g.53267361_53267365delinsTTTCC , CM000682.1:g.53267361_53267365delinsTTTCC	GRCh37
NC_000020.9:g.52700768_52700772delinsTTTCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262593.10:c.*343_*347delinsTTTCC MANE Select	ENSP00000262593.5:n.*343_*347delinsTTTCC
ENST00000262593.9:c.*343_*347delinsTTTCC	ENSP00000262593.5:n.*343_*347delinsTTTCC
ENST00000395939.5:c.*343_*347delinsTTTCC	ENSP00000379270.1:n.*343_*347delinsTTTCC
NM_018431.4:c.*343_*347delinsTTTCC	NP_060901.2:n.*343_*347delinsTTTCC
NM_177959.2:c.*343_*347delinsTTTCC	NP_808874.1:n.*343_*347delinsTTTCC
XM_011528903.1:c.*343_*347delinsTTTCC	XP_011527205.1:n.*343_*347delinsTTTCC
XM_011528904.1:c.*343_*347delinsTTTCC	XP_011527206.1:n.*343_*347delinsTTTCC
XM_024451946.1:c.*343_*347delinsTTTCC	XP_024307714.1:n.*343_*347delinsTTTCC
NM_018431.5:c.*343_*347delinsTTTCC MANE Select	NP_060901.2:n.*343_*347delinsTTTCC
NM_177959.3:c.*343_*347delinsTTTCC	NP_808874.1:n.*343_*347delinsTTTCC