Canonical Allele Identifier: CA1826874083
Gene: DOCK8 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.2175C= ENSP00000371766.2:p.His725=
ENST00000382331.6:n.876C=
ENST00000483757.6:c.*1066C= ENSP00000417691.2:n.*1066C=
ENST00000682260.1:n.2275C=
ENST00000685949.1:n.1167C=
ENST00000432829.7:c.2379C= MANE Select ENSP00000394888.3:p.His793=
ENST00000382329.1:c.780C= ENSP00000371766.1:p.His260=
ENST00000382331.5:c.285C= ENSP00000371768.1:p.His95=
ENST00000432829.6:c.2379C= ENSP00000394888.3:p.His793=
ENST00000453981.5:c.2175C= ENSP00000408464.2:p.His725=
ENST00000469391.5:c.2175C= ENSP00000419438.1:p.His725=
ENST00000483757.5:c.*1854C= ENSP00000417691.1:n.*1854C=
ENST00000495184.5:n.4334C=
NM_001190458.1:c.2175C= NP_001177387.1:p.His725=
NM_001193536.1:c.2175C= NP_001180465.1:p.His725=
NM_203447.3:c.2379C= , LRG_196t1:c.2379C= NP_982272.2:p.His793=
XM_011518045.1:c.2175C= XP_011516347.1:p.His725=
XM_011518046.1:c.2241C= XP_011516348.1:p.His747=
XM_011518047.1:c.2175C= XP_011516349.1:p.His725=
XM_011518048.1:c.2175C= XP_011516350.1:p.His725=
XM_011518049.1:c.615C= XP_011516351.1:p.His205=
XM_011518045.3:c.2175C= XP_011516347.1:p.His725=
XM_011518046.2:c.2241C= XP_011516348.1:p.His747=
XM_011518047.3:c.2175C= XP_011516349.1:p.His725=
XM_011518048.2:c.2175C= XP_011516350.1:p.His725=
XM_011518049.2:c.615C= XP_011516351.1:p.His205=
XM_017015173.1:c.2175C= XP_016870662.1:p.His725=
XM_017015174.1:c.2241C= XP_016870663.1:p.His747=
NM_001190458.2:c.2175C= NP_001177387.1:p.His725=
NM_001193536.2:c.2175C= NP_001180465.1:p.His725=
NM_203447.4:c.2379C= MANE Select NP_982272.2:p.His793=