Canonical Allele Identifier: CA1018606253
Gene: DOK5 HGNC NCBI

Linked Data

dbSNP Id: rs1875675905

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650563A>T , CM000682.2:g.54650563A>T GRCh38
NC_000020.10:g.53267102A>T , CM000682.1:g.53267102A>T GRCh37
NC_000020.9:g.52700509A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.*84A>T MANE Select ENSP00000262593.5:n.*84A>T
ENST00000262593.9:c.*84A>T ENSP00000262593.5:n.*84A>T
ENST00000395939.5:c.*84A>T ENSP00000379270.1:n.*84A>T
NM_018431.4:c.*84A>T NP_060901.2:n.*84A>T
NM_177959.2:c.*84A>T NP_808874.1:n.*84A>T
XM_011528903.1:c.*84A>T XP_011527205.1:n.*84A>T
XM_011528904.1:c.*84A>T XP_011527206.1:n.*84A>T
XM_024451946.1:c.*84A>T XP_024307714.1:n.*84A>T
NM_018431.5:c.*84A>T MANE Select NP_060901.2:n.*84A>T
NM_177959.3:c.*84A>T NP_808874.1:n.*84A>T