Canonical Allele Identifier: CA1826910655
Gene: DOCK8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.452094A= , CM000671.2:g.452094A= GRCh38
NC_000009.11:g.452094A= , CM000671.1:g.452094A= GRCh37
NC_000009.10:g.442094A= NCBI36
NG_017007.1:g.242230A= , LRG_196:g.242230A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382329.2:c.5745A= ENSP00000371766.2:p.Leu1915=
ENST00000683406.1:n.2520A=
ENST00000684637.1:n.1726A=
ENST00000685949.1:n.4833A=
ENST00000432829.7:c.6045A= MANE Select ENSP00000394888.3:p.Leu2015=
ENST00000382329.1:c.4446A= ENSP00000371766.1:p.Leu1482=
ENST00000432829.6:c.6045A= ENSP00000394888.3:p.Leu2015=
ENST00000453981.5:c.5841A= ENSP00000408464.2:p.Leu1947=
ENST00000469391.5:c.5745A= ENSP00000419438.1:p.Leu1915=
ENST00000495184.5:n.8000A=
NM_001190458.1:c.5745A= NP_001177387.1:p.Leu1915=
NM_001193536.1:c.5841A= NP_001180465.1:p.Leu1947=
NM_203447.3:c.6045A= , LRG_196t1:c.6045A= NP_982272.2:p.Leu2015=
XM_011518045.1:c.5745A= XP_011516347.1:p.Leu1915=
XM_011518046.1:c.5907A= XP_011516348.1:p.Leu1969=
XM_011518047.1:c.5841A= XP_011516349.1:p.Leu1947=
XM_011518048.1:c.5841A= XP_011516350.1:p.Leu1947=
XM_011518049.1:c.4281A= XP_011516351.1:p.Leu1427=
XM_011518045.3:c.5745A= XP_011516347.1:p.Leu1915=
XM_011518046.2:c.5907A= XP_011516348.1:p.Leu1969=
XM_011518047.3:c.5841A= XP_011516349.1:p.Leu1947=
XM_011518048.2:c.5841A= XP_011516350.1:p.Leu1947=
XM_011518049.2:c.4281A= XP_011516351.1:p.Leu1427=
XM_017015173.1:c.5841A= XP_016870662.1:p.Leu1947=
XM_017015174.1:c.5907A= XP_016870663.1:p.Leu1969=
NM_001190458.2:c.5745A= NP_001177387.1:p.Leu1915=
NM_001193536.2:c.5841A= NP_001180465.1:p.Leu1947=
NM_203447.4:c.6045A= MANE Select NP_982272.2:p.Leu2015=