Canonical Allele Identifier: CA4957710
Gene: DOCK8 HGNC NCBI
ClinVar Variation:
gnomAD v2:
gnomAD v3:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.336687C>A , CM000671.2:g.336687C>A GRCh38
NC_000009.11:g.336687C>A , CM000671.1:g.336687C>A GRCh37
NC_000009.10:g.326687C>A NCBI36
NG_017007.1:g.126823C>A , LRG_196:g.126823C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.1187C>A ENSP00000371766.2:p.Ser396Tyr
ENST00000483757.6:c.1187C>A ENSP00000417691.2:p.Ser396Tyr
ENST00000432829.7:c.1391C>A MANE Select ENSP00000394888.3:p.Ser464Tyr
ENST00000382341.5:n.1286C>A
ENST00000432829.6:c.1391C>A ENSP00000394888.3:p.Ser464Tyr
ENST00000453981.5:c.1187C>A ENSP00000408464.2:p.Ser396Tyr
ENST00000454469.6:n.1500C>A
ENST00000469391.5:c.1187C>A ENSP00000419438.1:p.Ser396Tyr
ENST00000483757.5:c.1187C>A ENSP00000417691.1:p.Ser396Tyr
ENST00000495184.5:n.1252C>A
ENST00000524396.5:c.*1354C>A ENSP00000436628.1:n.*1354C>A
NM_001190458.1:c.1187C>A NP_001177387.1:p.Ser396Tyr
NM_001193536.1:c.1187C>A NP_001180465.1:p.Ser396Tyr
NM_203447.3:c.1391C>A , LRG_196t1:c.1391C>A NP_982272.2:p.Ser464Tyr
XM_011518045.1:c.1187C>A XP_011516347.1:p.Ser396Tyr
XM_011518046.1:c.1253C>A XP_011516348.1:p.Ser418Tyr
XM_011518047.1:c.1187C>A XP_011516349.1:p.Ser396Tyr
XM_011518048.1:c.1187C>A XP_011516350.1:p.Ser396Tyr
XM_011518045.3:c.1187C>A XP_011516347.1:p.Ser396Tyr
XM_011518046.2:c.1253C>A XP_011516348.1:p.Ser418Tyr
XM_011518047.3:c.1187C>A XP_011516349.1:p.Ser396Tyr
XM_011518048.2:c.1187C>A XP_011516350.1:p.Ser396Tyr
XM_017015173.1:c.1187C>A XP_016870662.1:p.Ser396Tyr
XM_017015174.1:c.1253C>A XP_016870663.1:p.Ser418Tyr
NM_001190458.2:c.1187C>A NP_001177387.1:p.Ser396Tyr
NM_001193536.2:c.1187C>A NP_001180465.1:p.Ser396Tyr
NM_203447.4:c.1391C>A MANE Select NP_982272.2:p.Ser464Tyr