Canonical Allele Identifier: CA1826910633

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.452042C= , CM000671.2:g.452042C=	GRCh38
NC_000009.11:g.452042C= , CM000671.1:g.452042C=	GRCh37
NC_000009.10:g.442042C=	NCBI36
NG_017007.1:g.242178C= , LRG_196:g.242178C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5693C=	ENSP00000371766.2:p.Ala1898=
ENST00000683406.1:n.2468C=
ENST00000684637.1:n.1674C=
ENST00000685949.1:n.4781C=
ENST00000432829.7:c.5993C= MANE Select	ENSP00000394888.3:p.Ala1998=
ENST00000382329.1:c.4394C=	ENSP00000371766.1:p.Ala1465=
ENST00000432829.6:c.5993C=	ENSP00000394888.3:p.Ala1998=
ENST00000453981.5:c.5789C=	ENSP00000408464.2:p.Ala1930=
ENST00000469391.5:c.5693C=	ENSP00000419438.1:p.Ala1898=
ENST00000495184.5:n.7948C=
NM_001190458.1:c.5693C=	NP_001177387.1:p.Ala1898=
NM_001193536.1:c.5789C=	NP_001180465.1:p.Ala1930=
NM_203447.3:c.5993C= , LRG_196t1:c.5993C=	NP_982272.2:p.Ala1998=
XM_011518045.1:c.5693C=	XP_011516347.1:p.Ala1898=
XM_011518046.1:c.5855C=	XP_011516348.1:p.Ala1952=
XM_011518047.1:c.5789C=	XP_011516349.1:p.Ala1930=
XM_011518048.1:c.5789C=	XP_011516350.1:p.Ala1930=
XM_011518049.1:c.4229C=	XP_011516351.1:p.Ala1410=
XM_011518045.3:c.5693C=	XP_011516347.1:p.Ala1898=
XM_011518046.2:c.5855C=	XP_011516348.1:p.Ala1952=
XM_011518047.3:c.5789C=	XP_011516349.1:p.Ala1930=
XM_011518048.2:c.5789C=	XP_011516350.1:p.Ala1930=
XM_011518049.2:c.4229C=	XP_011516351.1:p.Ala1410=
XM_017015173.1:c.5789C=	XP_016870662.1:p.Ala1930=
XM_017015174.1:c.5855C=	XP_016870663.1:p.Ala1952=
NM_001190458.2:c.5693C=	NP_001177387.1:p.Ala1898=
NM_001193536.2:c.5789C=	NP_001180465.1:p.Ala1930=
NM_203447.4:c.5993C= MANE Select	NP_982272.2:p.Ala1998=