Canonical Allele Identifier: CA409691500

Gene: DOK5

Linked Data

• MyVariant Identifiers: chr20:g.53266953G>T (hg19) ; chr20:g.54650414G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54650414G>T , CM000682.2:g.54650414G>T	GRCh38
NC_000020.10:g.53266953G>T , CM000682.1:g.53266953G>T	GRCh37
NC_000020.9:g.52700360G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262593.10:c.857-1G>T MANE Select	ENSP00000262593.5:n.857-1G>T
ENST00000262593.9:c.857-1G>T	ENSP00000262593.5:n.857-1G>T
ENST00000395939.5:c.533-1G>T	ENSP00000379270.1:n.533-1G>T
NM_018431.4:c.857-1G>T	NP_060901.2:n.857-1G>T
NM_177959.2:c.533-1G>T	NP_808874.1:n.533-1G>T
XM_011528903.1:c.821-1G>T	XP_011527205.1:n.821-1G>T
XM_011528904.1:c.533-1G>T	XP_011527206.1:n.533-1G>T
XM_024451946.1:c.821-1G>T	XP_024307714.1:n.821-1G>T
NM_018431.5:c.857-1G>T MANE Select	NP_060901.2:n.857-1G>T
NM_177959.3:c.533-1G>T	NP_808874.1:n.533-1G>T