Canonical Allele Identifier: CA372760607
Gene: DOCK8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.414861A>T , CM000671.2:g.414861A>T GRCh38
NC_000009.11:g.414861A>T , CM000671.1:g.414861A>T GRCh37
NC_000009.10:g.404861A>T NCBI36
NG_017007.1:g.204997A>T , LRG_196:g.204997A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.3310A>T ENSP00000371766.2:p.Lys1104Ter
ENST00000683406.1:n.131A>T
ENST00000685949.1:n.2398A>T
ENST00000432829.7:c.3610A>T MANE Select ENSP00000394888.3:p.Lys1204Ter
ENST00000382329.1:c.2011A>T ENSP00000371766.1:p.Lys671Ter
ENST00000432829.6:c.3610A>T ENSP00000394888.3:p.Lys1204Ter
ENST00000453981.5:c.3406A>T ENSP00000408464.2:p.Lys1136Ter
ENST00000469391.5:c.3310A>T ENSP00000419438.1:p.Lys1104Ter
ENST00000495184.5:n.5565A>T
NM_001190458.1:c.3310A>T NP_001177387.1:p.Lys1104Ter
NM_001193536.1:c.3406A>T NP_001180465.1:p.Lys1136Ter
NM_203447.3:c.3610A>T , LRG_196t1:c.3610A>T NP_982272.2:p.Lys1204Ter
XM_011518045.1:c.3310A>T XP_011516347.1:p.Lys1104Ter
XM_011518046.1:c.3472A>T XP_011516348.1:p.Lys1158Ter
XM_011518047.1:c.3406A>T XP_011516349.1:p.Lys1136Ter
XM_011518048.1:c.3406A>T XP_011516350.1:p.Lys1136Ter
XM_011518049.1:c.1846A>T XP_011516351.1:p.Lys616Ter
XM_011518045.3:c.3310A>T XP_011516347.1:p.Lys1104Ter
XM_011518046.2:c.3472A>T XP_011516348.1:p.Lys1158Ter
XM_011518047.3:c.3406A>T XP_011516349.1:p.Lys1136Ter
XM_011518048.2:c.3406A>T XP_011516350.1:p.Lys1136Ter
XM_011518049.2:c.1846A>T XP_011516351.1:p.Lys616Ter
XM_017015173.1:c.3406A>T XP_016870662.1:p.Lys1136Ter
XM_017015174.1:c.3472A>T XP_016870663.1:p.Lys1158Ter
NM_001190458.2:c.3310A>T NP_001177387.1:p.Lys1104Ter
NM_001193536.2:c.3406A>T NP_001180465.1:p.Lys1136Ter
NM_203447.4:c.3610A>T MANE Select NP_982272.2:p.Lys1204Ter