Canonical Allele Identifier: CA1018606268

Gene: DOK5

Linked Data

• dbSNP Id: rs1600770580
• gnomAD v3: 20-54650630-C-A
• gnomAD v4: 20-54650630-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54650630C>A , CM000682.2:g.54650630C>A	GRCh38
NC_000020.10:g.53267169C>A , CM000682.1:g.53267169C>A	GRCh37
NC_000020.9:g.52700576C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262593.10:c.*151C>A MANE Select	ENSP00000262593.5:n.*151C>A
ENST00000262593.9:c.*151C>A	ENSP00000262593.5:n.*151C>A
ENST00000395939.5:c.*151C>A	ENSP00000379270.1:n.*151C>A
NM_018431.4:c.*151C>A	NP_060901.2:n.*151C>A
NM_177959.2:c.*151C>A	NP_808874.1:n.*151C>A
XM_011528903.1:c.*151C>A	XP_011527205.1:n.*151C>A
XM_011528904.1:c.*151C>A	XP_011527206.1:n.*151C>A
XM_024451946.1:c.*151C>A	XP_024307714.1:n.*151C>A
NM_018431.5:c.*151C>A MANE Select	NP_060901.2:n.*151C>A
NM_177959.3:c.*151C>A	NP_808874.1:n.*151C>A