Canonical Allele Identifier: CA372763383
Gene: DOCK8 HGNC NCBI

Linked Data

dbSNP Id: rs776951928
gnomAD v2: 9-377150-C-G
gnomAD v3: 9-377150-C-G
gnomAD v4: 9-377150-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.377150C>G , CM000671.2:g.377150C>G GRCh38
NC_000009.11:g.377150C>G , CM000671.1:g.377150C>G GRCh37
NC_000009.10:g.367150C>G NCBI36
NG_017007.1:g.167286C>G , LRG_196:g.167286C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.2175C>G ENSP00000371766.2:p.His725Gln
ENST00000382331.6:n.876C>G
ENST00000483757.6:c.*1066C>G ENSP00000417691.2:n.*1066C>G
ENST00000682260.1:n.2275C>G
ENST00000685949.1:n.1167C>G
ENST00000432829.7:c.2379C>G MANE Select ENSP00000394888.3:p.His793Gln
ENST00000382329.1:c.780C>G ENSP00000371766.1:p.His260Gln
ENST00000382331.5:c.285C>G ENSP00000371768.1:p.His95Gln
ENST00000432829.6:c.2379C>G ENSP00000394888.3:p.His793Gln
ENST00000453981.5:c.2175C>G ENSP00000408464.2:p.His725Gln
ENST00000469391.5:c.2175C>G ENSP00000419438.1:p.His725Gln
ENST00000483757.5:c.*1854C>G ENSP00000417691.1:n.*1854C>G
ENST00000495184.5:n.4334C>G
NM_001190458.1:c.2175C>G NP_001177387.1:p.His725Gln
NM_001193536.1:c.2175C>G NP_001180465.1:p.His725Gln
NM_203447.3:c.2379C>G , LRG_196t1:c.2379C>G NP_982272.2:p.His793Gln
XM_011518045.1:c.2175C>G XP_011516347.1:p.His725Gln
XM_011518046.1:c.2241C>G XP_011516348.1:p.His747Gln
XM_011518047.1:c.2175C>G XP_011516349.1:p.His725Gln
XM_011518048.1:c.2175C>G XP_011516350.1:p.His725Gln
XM_011518049.1:c.615C>G XP_011516351.1:p.His205Gln
XM_011518045.3:c.2175C>G XP_011516347.1:p.His725Gln
XM_011518046.2:c.2241C>G XP_011516348.1:p.His747Gln
XM_011518047.3:c.2175C>G XP_011516349.1:p.His725Gln
XM_011518048.2:c.2175C>G XP_011516350.1:p.His725Gln
XM_011518049.2:c.615C>G XP_011516351.1:p.His205Gln
XM_017015173.1:c.2175C>G XP_016870662.1:p.His725Gln
XM_017015174.1:c.2241C>G XP_016870663.1:p.His747Gln
NM_001190458.2:c.2175C>G NP_001177387.1:p.His725Gln
NM_001193536.2:c.2175C>G NP_001180465.1:p.His725Gln
NM_203447.4:c.2379C>G MANE Select NP_982272.2:p.His793Gln