Canonical Allele Identifier: CA745649992

Gene: DOK5

Linked Data

• dbSNP Id: rs1482932709
• MyVariant Identifiers: chr20:g.53267115_53267117del (hg19) ; chr20:g.54650576_54650578del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.54650581_54650583del , CM000682.2:g.54650581_54650583del	GRCh38
NC_000020.10:g.53267120_53267122del , CM000682.1:g.53267120_53267122del	GRCh37
NC_000020.9:g.52700527_52700529del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262593.10:c.*102_*104del MANE Select	ENSP00000262593.5:n.*102_*104del
ENST00000262593.9:c.*102_*104del	ENSP00000262593.5:n.*102_*104del
ENST00000395939.5:c.*102_*104del	ENSP00000379270.1:n.*102_*104del
NM_018431.4:c.*102_*104del	NP_060901.2:n.*102_*104del
NM_177959.2:c.*102_*104del	NP_808874.1:n.*102_*104del
XM_011528903.1:c.*102_*104del	XP_011527205.1:n.*102_*104del
XM_011528904.1:c.*102_*104del	XP_011527206.1:n.*102_*104del
XM_024451946.1:c.*102_*104del	XP_024307714.1:n.*102_*104del
NM_018431.5:c.*102_*104del MANE Select	NP_060901.2:n.*102_*104del
NM_177959.3:c.*102_*104del	NP_808874.1:n.*102_*104del