Canonical Allele Identifier: CA4958570
Gene: DOCK8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.399274dup , CM000671.2:g.399274dup GRCh38
NC_000009.11:g.399274dup , CM000671.1:g.399274dup GRCh37
NC_000009.10:g.389274dup NCBI36
NG_017007.1:g.189410dup , LRG_196:g.189410dup

Transcript Alleles

HGVS Amino-acid Change
NM_203447.4:c.3234+15dup MANE Select NP_982272.2:n.3234+15dup
ENST00000432829.7:c.3234+15dup MANE Select ENSP00000394888.3:n.3234+15dup
NM_001190458.1:c.2934+15dup NP_001177387.1:n.2934+15dup
NM_001190458.2:c.2934+15dup NP_001177387.1:n.2934+15dup
NM_001193536.1:c.3030+15dup NP_001180465.1:n.3030+15dup
NM_001193536.2:c.3030+15dup NP_001180465.1:n.3030+15dup
NM_203447.3:c.3234+15dup , LRG_196t1:c.3234+15dup NP_982272.2:n.3234+15dup
ENST00000382329.1:c.1635+15dup ENSP00000371766.1:n.1635+15dup
ENST00000382329.2:c.2934+15dup ENSP00000371766.2:n.2934+15dup
ENST00000382331.5:c.1140+15dup ENSP00000371768.1:n.1140+15dup
ENST00000382331.6:n.1731+15dup
ENST00000432829.6:c.3234+15dup ENSP00000394888.3:n.3234+15dup
ENST00000453981.5:c.3030+15dup ENSP00000408464.2:n.3030+15dup
ENST00000469391.5:c.2934+15dup ENSP00000419438.1:n.2934+15dup
ENST00000495184.5:n.5189+15dup
ENST00000682260.1:n.3145dup
ENST00000685949.1:n.2022+15dup
XM_011518045.1:c.2934+15dup XP_011516347.1:n.2934+15dup
XM_011518045.3:c.2934+15dup XP_011516347.1:n.2934+15dup
XM_011518046.1:c.3096+15dup XP_011516348.1:n.3096+15dup
XM_011518046.2:c.3096+15dup XP_011516348.1:n.3096+15dup
XM_011518047.1:c.3030+15dup XP_011516349.1:n.3030+15dup
XM_011518047.3:c.3030+15dup XP_011516349.1:n.3030+15dup
XM_011518048.1:c.3030+15dup XP_011516350.1:n.3030+15dup
XM_011518048.2:c.3030+15dup XP_011516350.1:n.3030+15dup
XM_011518049.1:c.1470+15dup XP_011516351.1:n.1470+15dup
XM_011518049.2:c.1470+15dup XP_011516351.1:n.1470+15dup
XM_017015173.1:c.3030+15dup XP_016870662.1:n.3030+15dup
XM_017015174.1:c.3096+15dup XP_016870663.1:n.3096+15dup