Canonical Allele Identifier: CA187777418
Gene: DOCK8 HGNC NCBI

Linked Data

dbSNP Id: rs111715716

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.414844T>A , CM000671.2:g.414844T>A GRCh38
NC_000009.11:g.414844T>A , CM000671.1:g.414844T>A GRCh37
NC_000009.10:g.404844T>A NCBI36
NG_017007.1:g.204980T>A , LRG_196:g.204980T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.3293T>A ENSP00000371766.2:p.Leu1098Gln
ENST00000683406.1:n.114T>A
ENST00000685949.1:n.2381T>A
ENST00000432829.7:c.3593T>A MANE Select ENSP00000394888.3:p.Leu1198Gln
ENST00000382329.1:c.1994T>A ENSP00000371766.1:p.Leu665Gln
ENST00000432829.6:c.3593T>A ENSP00000394888.3:p.Leu1198Gln
ENST00000453981.5:c.3389T>A ENSP00000408464.2:p.Leu1130Gln
ENST00000469391.5:c.3293T>A ENSP00000419438.1:p.Leu1098Gln
ENST00000495184.5:n.5548T>A
NM_001190458.1:c.3293T>A NP_001177387.1:p.Leu1098Gln
NM_001193536.1:c.3389T>A NP_001180465.1:p.Leu1130Gln
NM_203447.3:c.3593T>A , LRG_196t1:c.3593T>A NP_982272.2:p.Leu1198Gln
XM_011518045.1:c.3293T>A XP_011516347.1:p.Leu1098Gln
XM_011518046.1:c.3455T>A XP_011516348.1:p.Leu1152Gln
XM_011518047.1:c.3389T>A XP_011516349.1:p.Leu1130Gln
XM_011518048.1:c.3389T>A XP_011516350.1:p.Leu1130Gln
XM_011518049.1:c.1829T>A XP_011516351.1:p.Leu610Gln
XM_011518045.3:c.3293T>A XP_011516347.1:p.Leu1098Gln
XM_011518046.2:c.3455T>A XP_011516348.1:p.Leu1152Gln
XM_011518047.3:c.3389T>A XP_011516349.1:p.Leu1130Gln
XM_011518048.2:c.3389T>A XP_011516350.1:p.Leu1130Gln
XM_011518049.2:c.1829T>A XP_011516351.1:p.Leu610Gln
XM_017015173.1:c.3389T>A XP_016870662.1:p.Leu1130Gln
XM_017015174.1:c.3455T>A XP_016870663.1:p.Leu1152Gln
NM_001190458.2:c.3293T>A NP_001177387.1:p.Leu1098Gln
NM_001193536.2:c.3389T>A NP_001180465.1:p.Leu1130Gln
NM_203447.4:c.3593T>A MANE Select NP_982272.2:p.Leu1198Gln