Canonical Allele Identifier: CA1826910349
Gene: DOCK8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.451888_451906delinsTATATGCATATACATATAC , CM000671.2:g.451888_451906delinsTATATGCATATACATATAC GRCh38
NC_000009.11:g.451888_451906delinsTATATGCATATACATATAC , CM000671.1:g.451888_451906delinsTATATGCATATACATATAC GRCh37
NC_000009.10:g.441888_441906delinsTATATGCATATACATATAC NCBI36
NG_017007.1:g.242024_242042delinsTATATGCATATACATATAC , LRG_196:g.242024_242042delinsTATATGCATATACATATAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.5662-123_5662-105delinsTATATGCATATACATATAC ENSP00000371766.2:n.5662-123_5662-105delinsTATATGCATATACATATA...
ENST00000683406.1:n.2437-123_2437-105delinsTATATGCATATACATATAC
ENST00000684637.1:n.1643-123_1643-105delinsTATATGCATATACATATAC
ENST00000685949.1:n.4750-123_4750-105delinsTATATGCATATACATATAC
ENST00000432829.7:c.5962-123_5962-105delinsTATATGCATATACATATAC MANE Select ENSP00000394888.3:n.5962-123_5962-105delinsTATATGCATATACATATA...
ENST00000382329.1:c.4363-123_4363-105delinsTATATGCATATACATATAC ENSP00000371766.1:n.4363-123_4363-105delinsTATATGCATATACATATA...
ENST00000432829.6:c.5962-123_5962-105delinsTATATGCATATACATATAC ENSP00000394888.3:n.5962-123_5962-105delinsTATATGCATATACATATA...
ENST00000453981.5:c.5758-123_5758-105delinsTATATGCATATACATATAC ENSP00000408464.2:n.5758-123_5758-105delinsTATATGCATATACATATA...
ENST00000469391.5:c.5662-123_5662-105delinsTATATGCATATACATATAC ENSP00000419438.1:n.5662-123_5662-105delinsTATATGCATATACATATA...
ENST00000495184.5:n.7917-123_7917-105delinsTATATGCATATACATATAC
NM_001190458.1:c.5662-123_5662-105delinsTATATGCATATACATATAC NP_001177387.1:n.5662-123_5662-105delinsTATATGCATATACATATAC
NM_001193536.1:c.5758-123_5758-105delinsTATATGCATATACATATAC NP_001180465.1:n.5758-123_5758-105delinsTATATGCATATACATATAC
NM_203447.3:c.5962-123_5962-105delinsTATATGCATATACATATAC , LRG_196t1:c.5962-123_5962-105delinsTATATGCATATACATATAC NP_982272.2:n.5962-123_5962-105delinsTATATGCATATACATATAC
XM_011518045.1:c.5662-123_5662-105delinsTATATGCATATACATATAC XP_011516347.1:n.5662-123_5662-105delinsTATATGCATATACATATAC
XM_011518046.1:c.5824-123_5824-105delinsTATATGCATATACATATAC XP_011516348.1:n.5824-123_5824-105delinsTATATGCATATACATATAC
XM_011518047.1:c.5758-123_5758-105delinsTATATGCATATACATATAC XP_011516349.1:n.5758-123_5758-105delinsTATATGCATATACATATAC
XM_011518048.1:c.5758-123_5758-105delinsTATATGCATATACATATAC XP_011516350.1:n.5758-123_5758-105delinsTATATGCATATACATATAC
XM_011518049.1:c.4198-123_4198-105delinsTATATGCATATACATATAC XP_011516351.1:n.4198-123_4198-105delinsTATATGCATATACATATAC
XM_011518045.3:c.5662-123_5662-105delinsTATATGCATATACATATAC XP_011516347.1:n.5662-123_5662-105delinsTATATGCATATACATATAC
XM_011518046.2:c.5824-123_5824-105delinsTATATGCATATACATATAC XP_011516348.1:n.5824-123_5824-105delinsTATATGCATATACATATAC
XM_011518047.3:c.5758-123_5758-105delinsTATATGCATATACATATAC XP_011516349.1:n.5758-123_5758-105delinsTATATGCATATACATATAC
XM_011518048.2:c.5758-123_5758-105delinsTATATGCATATACATATAC XP_011516350.1:n.5758-123_5758-105delinsTATATGCATATACATATAC
XM_011518049.2:c.4198-123_4198-105delinsTATATGCATATACATATAC XP_011516351.1:n.4198-123_4198-105delinsTATATGCATATACATATAC
XM_017015173.1:c.5758-123_5758-105delinsTATATGCATATACATATAC XP_016870662.1:n.5758-123_5758-105delinsTATATGCATATACATATAC
XM_017015174.1:c.5824-123_5824-105delinsTATATGCATATACATATAC XP_016870663.1:n.5824-123_5824-105delinsTATATGCATATACATATAC
NM_001190458.2:c.5662-123_5662-105delinsTATATGCATATACATATAC NP_001177387.1:n.5662-123_5662-105delinsTATATGCATATACATATAC
NM_001193536.2:c.5758-123_5758-105delinsTATATGCATATACATATAC NP_001180465.1:n.5758-123_5758-105delinsTATATGCATATACATATAC
NM_203447.4:c.5962-123_5962-105delinsTATATGCATATACATATAC MANE Select NP_982272.2:n.5962-123_5962-105delinsTATATGCATATACATATAC