Canonical Allele Identifier: CA372760727
Gene: DOCK8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.414880A>C , CM000671.2:g.414880A>C GRCh38
NC_000009.11:g.414880A>C , CM000671.1:g.414880A>C GRCh37
NC_000009.10:g.404880A>C NCBI36
NG_017007.1:g.205016A>C , LRG_196:g.205016A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.3329A>C ENSP00000371766.2:p.Lys1110Thr
ENST00000683406.1:n.150A>C
ENST00000685949.1:n.2417A>C
ENST00000432829.7:c.3629A>C MANE Select ENSP00000394888.3:p.Lys1210Thr
ENST00000382329.1:c.2030A>C ENSP00000371766.1:p.Lys677Thr
ENST00000432829.6:c.3629A>C ENSP00000394888.3:p.Lys1210Thr
ENST00000453981.5:c.3425A>C ENSP00000408464.2:p.Lys1142Thr
ENST00000469391.5:c.3329A>C ENSP00000419438.1:p.Lys1110Thr
ENST00000495184.5:n.5584A>C
NM_001190458.1:c.3329A>C NP_001177387.1:p.Lys1110Thr
NM_001193536.1:c.3425A>C NP_001180465.1:p.Lys1142Thr
NM_203447.3:c.3629A>C , LRG_196t1:c.3629A>C NP_982272.2:p.Lys1210Thr
XM_011518045.1:c.3329A>C XP_011516347.1:p.Lys1110Thr
XM_011518046.1:c.3491A>C XP_011516348.1:p.Lys1164Thr
XM_011518047.1:c.3425A>C XP_011516349.1:p.Lys1142Thr
XM_011518048.1:c.3425A>C XP_011516350.1:p.Lys1142Thr
XM_011518049.1:c.1865A>C XP_011516351.1:p.Lys622Thr
XM_011518045.3:c.3329A>C XP_011516347.1:p.Lys1110Thr
XM_011518046.2:c.3491A>C XP_011516348.1:p.Lys1164Thr
XM_011518047.3:c.3425A>C XP_011516349.1:p.Lys1142Thr
XM_011518048.2:c.3425A>C XP_011516350.1:p.Lys1142Thr
XM_011518049.2:c.1865A>C XP_011516351.1:p.Lys622Thr
XM_017015173.1:c.3425A>C XP_016870662.1:p.Lys1142Thr
XM_017015174.1:c.3491A>C XP_016870663.1:p.Lys1164Thr
NM_001190458.2:c.3329A>C NP_001177387.1:p.Lys1110Thr
NM_001193536.2:c.3425A>C NP_001180465.1:p.Lys1142Thr
NM_203447.4:c.3629A>C MANE Select NP_982272.2:p.Lys1210Thr