Canonical Allele Identifier: CA1826910637

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.452054C= , CM000671.2:g.452054C=	GRCh38
NC_000009.11:g.452054C= , CM000671.1:g.452054C=	GRCh37
NC_000009.10:g.442054C=	NCBI36
NG_017007.1:g.242190C= , LRG_196:g.242190C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.5705C=	ENSP00000371766.2:p.Ala1902=
ENST00000683406.1:n.2480C=
ENST00000684637.1:n.1686C=
ENST00000685949.1:n.4793C=
ENST00000432829.7:c.6005C= MANE Select	ENSP00000394888.3:p.Ala2002=
ENST00000382329.1:c.4406C=	ENSP00000371766.1:p.Ala1469=
ENST00000432829.6:c.6005C=	ENSP00000394888.3:p.Ala2002=
ENST00000453981.5:c.5801C=	ENSP00000408464.2:p.Ala1934=
ENST00000469391.5:c.5705C=	ENSP00000419438.1:p.Ala1902=
ENST00000495184.5:n.7960C=
NM_001190458.1:c.5705C=	NP_001177387.1:p.Ala1902=
NM_001193536.1:c.5801C=	NP_001180465.1:p.Ala1934=
NM_203447.3:c.6005C= , LRG_196t1:c.6005C=	NP_982272.2:p.Ala2002=
XM_011518045.1:c.5705C=	XP_011516347.1:p.Ala1902=
XM_011518046.1:c.5867C=	XP_011516348.1:p.Ala1956=
XM_011518047.1:c.5801C=	XP_011516349.1:p.Ala1934=
XM_011518048.1:c.5801C=	XP_011516350.1:p.Ala1934=
XM_011518049.1:c.4241C=	XP_011516351.1:p.Ala1414=
XM_011518045.3:c.5705C=	XP_011516347.1:p.Ala1902=
XM_011518046.2:c.5867C=	XP_011516348.1:p.Ala1956=
XM_011518047.3:c.5801C=	XP_011516349.1:p.Ala1934=
XM_011518048.2:c.5801C=	XP_011516350.1:p.Ala1934=
XM_011518049.2:c.4241C=	XP_011516351.1:p.Ala1414=
XM_017015173.1:c.5801C=	XP_016870662.1:p.Ala1934=
XM_017015174.1:c.5867C=	XP_016870663.1:p.Ala1956=
NM_001190458.2:c.5705C=	NP_001177387.1:p.Ala1902=
NM_001193536.2:c.5801C=	NP_001180465.1:p.Ala1934=
NM_203447.4:c.6005C= MANE Select	NP_982272.2:p.Ala2002=