Canonical Allele Identifier: CA1826888843
Gene: DOCK8 HGNC NCBI

Linked Data

dbSNP Id: rs2055903389
gnomAD v4: 9-414704-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.414704A>G , CM000671.2:g.414704A>G GRCh38
NC_000009.11:g.414704A>G , CM000671.1:g.414704A>G GRCh37
NC_000009.10:g.404704A>G NCBI36
NG_017007.1:g.204840A>G , LRG_196:g.204840A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.3231-78A>G ENSP00000371766.2:n.3231-78A>G
ENST00000683406.1:n.52-78A>G
ENST00000685949.1:n.2319-78A>G
ENST00000432829.7:c.3531-78A>G MANE Select ENSP00000394888.3:n.3531-78A>G
ENST00000382329.1:c.1932-78A>G ENSP00000371766.1:n.1932-78A>G
ENST00000432829.6:c.3531-78A>G ENSP00000394888.3:n.3531-78A>G
ENST00000453981.5:c.3327-78A>G ENSP00000408464.2:n.3327-78A>G
ENST00000469391.5:c.3231-78A>G ENSP00000419438.1:n.3231-78A>G
ENST00000495184.5:n.5486-78A>G
NM_001190458.1:c.3231-78A>G NP_001177387.1:n.3231-78A>G
NM_001193536.1:c.3327-78A>G NP_001180465.1:n.3327-78A>G
NM_203447.3:c.3531-78A>G , LRG_196t1:c.3531-78A>G NP_982272.2:n.3531-78A>G
XM_011518045.1:c.3231-78A>G XP_011516347.1:n.3231-78A>G
XM_011518046.1:c.3393-78A>G XP_011516348.1:n.3393-78A>G
XM_011518047.1:c.3327-78A>G XP_011516349.1:n.3327-78A>G
XM_011518048.1:c.3327-78A>G XP_011516350.1:n.3327-78A>G
XM_011518049.1:c.1767-78A>G XP_011516351.1:n.1767-78A>G
XM_011518045.3:c.3231-78A>G XP_011516347.1:n.3231-78A>G
XM_011518046.2:c.3393-78A>G XP_011516348.1:n.3393-78A>G
XM_011518047.3:c.3327-78A>G XP_011516349.1:n.3327-78A>G
XM_011518048.2:c.3327-78A>G XP_011516350.1:n.3327-78A>G
XM_011518049.2:c.1767-78A>G XP_011516351.1:n.1767-78A>G
XM_017015173.1:c.3327-78A>G XP_016870662.1:n.3327-78A>G
XM_017015174.1:c.3393-78A>G XP_016870663.1:n.3393-78A>G
NM_001190458.2:c.3231-78A>G NP_001177387.1:n.3231-78A>G
NM_001193536.2:c.3327-78A>G NP_001180465.1:n.3327-78A>G
NM_203447.4:c.3531-78A>G MANE Select NP_982272.2:n.3531-78A>G