Canonical Allele Identifier: CA1826807531
Gene: DOCK8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.271530G= , CM000671.2:g.271530G= GRCh38
NC_000009.11:g.271530G= , CM000671.1:g.271530G= GRCh37
NC_000009.10:g.261530G= NCBI36
NG_017007.1:g.61666G= , LRG_196:g.61666G=

Transcript Alleles

HGVS Amino-acid change
ENST00000382329.2:c.-151-97G= ENSP00000371766.2:n.-151-97G=
ENST00000682121.1:n.166-14931G=
ENST00000684166.1:n.163-97G=
ENST00000684384.1:n.163-97G=
ENST00000432829.7:c.54-97G= MANE Select ENSP00000394888.3:n.54-97G=
ENST00000432829.6:c.54-97G= ENSP00000394888.3:n.54-97G=
ENST00000454469.6:n.163-97G=
ENST00000469197.5:c.54-97G= ENSP00000418587.1:n.54-97G=
ENST00000479404.5:c.-151-97G= ENSP00000417082.1:n.-151-97G=
ENST00000524396.5:c.*17-97G= ENSP00000436628.1:n.*17-97G=
NM_203447.3:c.54-97G= , LRG_196t1:c.54-97G= NP_982272.2:n.54-97G=
XM_011518047.1:c.-151-97G= XP_011516349.1:n.-151-97G=
XR_929404.1:n.88+1375C=
XR_929406.1:n.1333+2754C=
XM_011518045.3:c.-151-97G= XP_011516347.1:n.-151-97G=
XM_011518047.3:c.-151-97G= XP_011516349.1:n.-151-97G=
XM_017015173.1:c.-151-97G= XP_016870662.1:n.-151-97G=
NM_203447.4:c.54-97G= MANE Select NP_982272.2:n.54-97G=