Canonical Allele Identifier: CA1826874008
Gene: DOCK8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.376989G= , CM000671.2:g.376989G= GRCh38
NC_000009.11:g.376989G= , CM000671.1:g.376989G= GRCh37
NC_000009.10:g.366989G= NCBI36
NG_017007.1:g.167125G= , LRG_196:g.167125G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.2014G= ENSP00000371766.2:p.Glu672=
ENST00000382331.6:n.715G=
ENST00000483757.6:c.*905G= ENSP00000417691.2:n.*905G=
ENST00000682260.1:n.2114G=
ENST00000685949.1:n.1006G=
ENST00000432829.7:c.2218G= MANE Select ENSP00000394888.3:p.Glu740=
ENST00000382329.1:c.619G= ENSP00000371766.1:p.Glu207=
ENST00000382331.5:c.124G= ENSP00000371768.1:p.Glu42=
ENST00000432829.6:c.2218G= ENSP00000394888.3:p.Glu740=
ENST00000453981.5:c.2014G= ENSP00000408464.2:p.Glu672=
ENST00000469391.5:c.2014G= ENSP00000419438.1:p.Glu672=
ENST00000483757.5:c.*1693G= ENSP00000417691.1:n.*1693G=
ENST00000495184.5:n.4173G=
NM_001190458.1:c.2014G= NP_001177387.1:p.Glu672=
NM_001193536.1:c.2014G= NP_001180465.1:p.Glu672=
NM_203447.3:c.2218G= , LRG_196t1:c.2218G= NP_982272.2:p.Glu740=
XM_011518045.1:c.2014G= XP_011516347.1:p.Glu672=
XM_011518046.1:c.2080G= XP_011516348.1:p.Glu694=
XM_011518047.1:c.2014G= XP_011516349.1:p.Glu672=
XM_011518048.1:c.2014G= XP_011516350.1:p.Glu672=
XM_011518049.1:c.454G= XP_011516351.1:p.Glu152=
XM_011518045.3:c.2014G= XP_011516347.1:p.Glu672=
XM_011518046.2:c.2080G= XP_011516348.1:p.Glu694=
XM_011518047.3:c.2014G= XP_011516349.1:p.Glu672=
XM_011518048.2:c.2014G= XP_011516350.1:p.Glu672=
XM_011518049.2:c.454G= XP_011516351.1:p.Glu152=
XM_017015173.1:c.2014G= XP_016870662.1:p.Glu672=
XM_017015174.1:c.2080G= XP_016870663.1:p.Glu694=
NM_001190458.2:c.2014G= NP_001177387.1:p.Glu672=
NM_001193536.2:c.2014G= NP_001180465.1:p.Glu672=
NM_203447.4:c.2218G= MANE Select NP_982272.2:p.Glu740=