Canonical Allele Identifier: CA2582489471
Gene: DOCK6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.11200542_11200622del , CM000681.2:g.11200542_11200622del GRCh38
NC_000019.9:g.11311218_11311298del , CM000681.1:g.11311218_11311298del GRCh37
NC_000019.8:g.11172218_11172298del NCBI36
NG_031953.1:g.66876_66956del
NG_051186.1:g.1951_2031del

Transcript Alleles

HGVS Amino-acid Change
ENST00000587656.6:c.6044+99_6045-68del ENSP00000468638.2:n.6044+99_6045-68del
ENST00000294618.12:c.5939+99_5940-68del MANE Select ENSP00000294618.6:n.5939+99_5940-68del
ENST00000294618.11:c.5939+99_5940-68del ENSP00000294618.6:n.5939+99_5940-68del
ENST00000586702.1:n.842+99_843-68del
ENST00000587656.5:c.3804+99_3805-68del
ENST00000587734.1:c.76-1078_76-998del ENSP00000468291.1:n.76-1078_76-998del
NM_020812.3:c.5939+99_5940-68del NP_065863.2:n.5939+99_5940-68del
XM_005260000.2:c.6137+99_6138-68del XP_005260057.1:n.6137+99_6138-68del
XM_005260001.2:c.6044+99_6045-68del XP_005260058.1:n.6044+99_6045-68del
XM_006722804.2:c.3275+99_3276-68del XP_006722867.1:n.3275+99_3276-68del
XM_011528150.1:c.6077+99_6078-68del XP_011526452.1:n.6077+99_6078-68del
XM_011528151.1:c.6065+99_6066-68del XP_011526453.1:n.6065+99_6066-68del
XM_011528152.1:c.5972+99_5973-68del XP_011526454.1:n.5972+99_5973-68del
XR_936195.1:n.6184+99_6185-68del
XM_006722804.3:c.3275+99_3276-68del XP_006722867.1:n.3275+99_3276-68del
NM_001367830.1:c.6044+99_6045-68del NP_001354759.1:n.6044+99_6045-68del
NM_020812.4:c.5939+99_5940-68del MANE Select NP_065863.2:n.5939+99_5940-68del