Canonical Allele Identifier: CA2816747388
Gene: DOK5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.54650791_54650803dup , CM000682.2:g.54650791_54650803dup GRCh38
NC_000020.10:g.53267330_53267342dup , CM000682.1:g.53267330_53267342dup GRCh37
NC_000020.9:g.52700737_52700749dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262593.10:c.*312_*324dup MANE Select ENSP00000262593.5:n.*312_*324dup
ENST00000262593.9:c.*312_*324dup ENSP00000262593.5:n.*312_*324dup
ENST00000395939.5:c.*312_*324dup ENSP00000379270.1:n.*312_*324dup
NM_018431.4:c.*312_*324dup NP_060901.2:n.*312_*324dup
NM_177959.2:c.*312_*324dup NP_808874.1:n.*312_*324dup
XM_011528903.1:c.*312_*324dup XP_011527205.1:n.*312_*324dup
XM_011528904.1:c.*312_*324dup XP_011527206.1:n.*312_*324dup
XM_024451946.1:c.*312_*324dup XP_024307714.1:n.*312_*324dup
NM_018431.5:c.*312_*324dup MANE Select NP_060901.2:n.*312_*324dup
NM_177959.3:c.*312_*324dup NP_808874.1:n.*312_*324dup