Canonical Allele Identifier: CA1826910518
Gene: DOCK8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.451971_451991delinsATATATATTTTTTTTTTTTTT , CM000671.2:g.451971_451991delinsATATATATTTTTTTTTTTTTT GRCh38
NC_000009.11:g.451971_451991delinsATATATATTTTTTTTTTTTTT , CM000671.1:g.451971_451991delinsATATATATTTTTTTTTTTTTT GRCh37
NC_000009.10:g.441971_441991delinsATATATATTTTTTTTTTTTTT NCBI36
NG_017007.1:g.242107_242127delinsATATATATTTTTTTTTTTTTT , LRG_196:g.242107_242127delinsATATATATTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.5662-40_5662-20delinsATATATATTTTTTTTTTTTTT ENSP00000371766.2:n.5662-40_5662-20delinsATATATATTTTTTTTTTTTT...
ENST00000683406.1:n.2437-40_2437-20delinsATATATATTTTTTTTTTTTTT
ENST00000684637.1:n.1643-40_1643-20delinsATATATATTTTTTTTTTTTTT
ENST00000685949.1:n.4750-40_4750-20delinsATATATATTTTTTTTTTTTTT
ENST00000432829.7:c.5962-40_5962-20delinsATATATATTTTTTTTTTTTTT MANE Select ENSP00000394888.3:n.5962-40_5962-20delinsATATATATTTTTTTTTTTTT...
ENST00000382329.1:c.4363-40_4363-20delinsATATATATTTTTTTTTTTTTT ENSP00000371766.1:n.4363-40_4363-20delinsATATATATTTTTTTTTTTTT...
ENST00000432829.6:c.5962-40_5962-20delinsATATATATTTTTTTTTTTTTT ENSP00000394888.3:n.5962-40_5962-20delinsATATATATTTTTTTTTTTTT...
ENST00000453981.5:c.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT ENSP00000408464.2:n.5758-40_5758-20delinsATATATATTTTTTTTTTTTT...
ENST00000469391.5:c.5662-40_5662-20delinsATATATATTTTTTTTTTTTTT ENSP00000419438.1:n.5662-40_5662-20delinsATATATATTTTTTTTTTTTT...
ENST00000495184.5:n.7917-40_7917-20delinsATATATATTTTTTTTTTTTTT
NM_001190458.1:c.5662-40_5662-20delinsATATATATTTTTTTTTTTTTT NP_001177387.1:n.5662-40_5662-20delinsATATATATTTTTTTTTTTTTT
NM_001193536.1:c.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT NP_001180465.1:n.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT
NM_203447.3:c.5962-40_5962-20delinsATATATATTTTTTTTTTTTTT , LRG_196t1:c.5962-40_5962-20delinsATATATATTTTTTTTTTTTTT NP_982272.2:n.5962-40_5962-20delinsATATATATTTTTTTTTTTTTT
XM_011518045.1:c.5662-40_5662-20delinsATATATATTTTTTTTTTTTTT XP_011516347.1:n.5662-40_5662-20delinsATATATATTTTTTTTTTTTTT
XM_011518046.1:c.5824-40_5824-20delinsATATATATTTTTTTTTTTTTT XP_011516348.1:n.5824-40_5824-20delinsATATATATTTTTTTTTTTTTT
XM_011518047.1:c.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT XP_011516349.1:n.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT
XM_011518048.1:c.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT XP_011516350.1:n.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT
XM_011518049.1:c.4198-40_4198-20delinsATATATATTTTTTTTTTTTTT XP_011516351.1:n.4198-40_4198-20delinsATATATATTTTTTTTTTTTTT
XM_011518045.3:c.5662-40_5662-20delinsATATATATTTTTTTTTTTTTT XP_011516347.1:n.5662-40_5662-20delinsATATATATTTTTTTTTTTTTT
XM_011518046.2:c.5824-40_5824-20delinsATATATATTTTTTTTTTTTTT XP_011516348.1:n.5824-40_5824-20delinsATATATATTTTTTTTTTTTTT
XM_011518047.3:c.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT XP_011516349.1:n.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT
XM_011518048.2:c.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT XP_011516350.1:n.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT
XM_011518049.2:c.4198-40_4198-20delinsATATATATTTTTTTTTTTTTT XP_011516351.1:n.4198-40_4198-20delinsATATATATTTTTTTTTTTTTT
XM_017015173.1:c.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT XP_016870662.1:n.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT
XM_017015174.1:c.5824-40_5824-20delinsATATATATTTTTTTTTTTTTT XP_016870663.1:n.5824-40_5824-20delinsATATATATTTTTTTTTTTTTT
NM_001190458.2:c.5662-40_5662-20delinsATATATATTTTTTTTTTTTTT NP_001177387.1:n.5662-40_5662-20delinsATATATATTTTTTTTTTTTTT
NM_001193536.2:c.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT NP_001180465.1:n.5758-40_5758-20delinsATATATATTTTTTTTTTTTTT
NM_203447.4:c.5962-40_5962-20delinsATATATATTTTTTTTTTTTTT MANE Select NP_982272.2:n.5962-40_5962-20delinsATATATATTTTTTTTTTTTTT