Canonical Allele Identifier: CA1826889119

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414888G= , CM000671.2:g.414888G=	GRCh38
NC_000009.11:g.414888G= , CM000671.1:g.414888G=	GRCh37
NC_000009.10:g.404888G=	NCBI36
NG_017007.1:g.205024G= , LRG_196:g.205024G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3337G=	ENSP00000371766.2:p.Ala1113=
ENST00000683406.1:n.158G=
ENST00000685949.1:n.2425G=
ENST00000432829.7:c.3637G= MANE Select	ENSP00000394888.3:p.Ala1213=
ENST00000382329.1:c.2038G=	ENSP00000371766.1:p.Ala680=
ENST00000432829.6:c.3637G=	ENSP00000394888.3:p.Ala1213=
ENST00000453981.5:c.3433G=	ENSP00000408464.2:p.Ala1145=
ENST00000469391.5:c.3337G=	ENSP00000419438.1:p.Ala1113=
ENST00000495184.5:n.5592G=
NM_001190458.1:c.3337G=	NP_001177387.1:p.Ala1113=
NM_001193536.1:c.3433G=	NP_001180465.1:p.Ala1145=
NM_203447.3:c.3637G= , LRG_196t1:c.3637G=	NP_982272.2:p.Ala1213=
XM_011518045.1:c.3337G=	XP_011516347.1:p.Ala1113=
XM_011518046.1:c.3499G=	XP_011516348.1:p.Ala1167=
XM_011518047.1:c.3433G=	XP_011516349.1:p.Ala1145=
XM_011518048.1:c.3433G=	XP_011516350.1:p.Ala1145=
XM_011518049.1:c.1873G=	XP_011516351.1:p.Ala625=
XM_011518045.3:c.3337G=	XP_011516347.1:p.Ala1113=
XM_011518046.2:c.3499G=	XP_011516348.1:p.Ala1167=
XM_011518047.3:c.3433G=	XP_011516349.1:p.Ala1145=
XM_011518048.2:c.3433G=	XP_011516350.1:p.Ala1145=
XM_011518049.2:c.1873G=	XP_011516351.1:p.Ala625=
XM_017015173.1:c.3433G=	XP_016870662.1:p.Ala1145=
XM_017015174.1:c.3499G=	XP_016870663.1:p.Ala1167=
NM_001190458.2:c.3337G=	NP_001177387.1:p.Ala1113=
NM_001193536.2:c.3433G=	NP_001180465.1:p.Ala1145=
NM_203447.4:c.3637G= MANE Select	NP_982272.2:p.Ala1213=