Canonical Allele Identifier: CA1826845098

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.331427C= , CM000671.2:g.331427C=	GRCh38
NC_000009.11:g.331427C= , CM000671.1:g.331427C=	GRCh37
NC_000009.10:g.321427C=	NCBI36
NG_017007.1:g.121563C= , LRG_196:g.121563C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000382329.2:c.841-971C=	ENSP00000371766.2:n.841-971C=
ENST00000483757.6:c.841-971C=	ENSP00000417691.2:n.841-971C=
ENST00000432829.7:c.1045-971C= MANE Select	ENSP00000394888.3:n.1045-971C=
ENST00000382341.5:n.940-971C=
ENST00000432829.6:c.1045-971C=	ENSP00000394888.3:n.1045-971C=
ENST00000453981.5:c.841-971C=	ENSP00000408464.2:n.841-971C=
ENST00000454469.6:n.1154-971C=
ENST00000469391.5:c.841-971C=	ENSP00000419438.1:n.841-971C=
ENST00000483757.5:c.841-971C=	ENSP00000417691.1:n.841-971C=
ENST00000495184.5:n.906-971C=
ENST00000524396.5:c.*1008-971C=	ENSP00000436628.1:n.*1008-971C=
NM_001190458.1:c.841-971C=	NP_001177387.1:n.841-971C=
NM_001193536.1:c.841-971C=	NP_001180465.1:n.841-971C=
NM_203447.3:c.1045-971C= , LRG_196t1:c.1045-971C=	NP_982272.2:n.1045-971C=
XM_011518045.1:c.841-971C=	XP_011516347.1:n.841-971C=
XM_011518046.1:c.907-971C=	XP_011516348.1:n.907-971C=
XM_011518047.1:c.841-971C=	XP_011516349.1:n.841-971C=
XM_011518048.1:c.841-971C=	XP_011516350.1:n.841-971C=
XM_011518045.3:c.841-971C=	XP_011516347.1:n.841-971C=
XM_011518046.2:c.907-971C=	XP_011516348.1:n.907-971C=
XM_011518047.3:c.841-971C=	XP_011516349.1:n.841-971C=
XM_011518048.2:c.841-971C=	XP_011516350.1:n.841-971C=
XM_017015173.1:c.841-971C=	XP_016870662.1:n.841-971C=
XM_017015174.1:c.907-971C=	XP_016870663.1:n.907-971C=
NM_001190458.2:c.841-971C=	NP_001177387.1:n.841-971C=
NM_001193536.2:c.841-971C=	NP_001180465.1:n.841-971C=
NM_203447.4:c.1045-971C= MANE Select	NP_982272.2:n.1045-971C=