Canonical Allele Identifier: CA2370487830

Gene: DOK5

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54650402_54650403delinsCT , CM000682.2:g.54650402_54650403delinsCT	GRCh38
NC_000020.10:g.53266941_53266942delinsCT , CM000682.1:g.53266941_53266942delinsCT	GRCh37
NC_000020.9:g.52700348_52700349delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262593.10:c.857-13_857-12delinsCT MANE Select	ENSP00000262593.5:n.857-13_857-12delinsCT
ENST00000262593.9:c.857-13_857-12delinsCT	ENSP00000262593.5:n.857-13_857-12delinsCT
ENST00000395939.5:c.533-13_533-12delinsCT	ENSP00000379270.1:n.533-13_533-12delinsCT
NM_018431.4:c.857-13_857-12delinsCT	NP_060901.2:n.857-13_857-12delinsCT
NM_177959.2:c.533-13_533-12delinsCT	NP_808874.1:n.533-13_533-12delinsCT
XM_011528903.1:c.821-13_821-12delinsCT	XP_011527205.1:n.821-13_821-12delinsCT
XM_011528904.1:c.533-13_533-12delinsCT	XP_011527206.1:n.533-13_533-12delinsCT
XM_024451946.1:c.821-13_821-12delinsCT	XP_024307714.1:n.821-13_821-12delinsCT
NM_018431.5:c.857-13_857-12delinsCT MANE Select	NP_060901.2:n.857-13_857-12delinsCT
NM_177959.3:c.533-13_533-12delinsCT	NP_808874.1:n.533-13_533-12delinsCT