Canonical Allele Identifier: CA1826902154

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.441331C= , CM000671.2:g.441331C=	GRCh38
NC_000009.11:g.441331C= , CM000671.1:g.441331C=	GRCh37
NC_000009.10:g.431331C=	NCBI36
NG_017007.1:g.231467C= , LRG_196:g.231467C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.4969C=	ENSP00000371766.2:p.Pro1657=
ENST00000683406.1:n.1744C=
ENST00000684637.1:n.950C=
ENST00000685949.1:n.4057C=
ENST00000432829.7:c.5269C= MANE Select	ENSP00000394888.3:p.Pro1757=
ENST00000382329.1:c.3670C=	ENSP00000371766.1:p.Pro1224=
ENST00000432829.6:c.5269C=	ENSP00000394888.3:p.Pro1757=
ENST00000453981.5:c.5065C=	ENSP00000408464.2:p.Pro1689=
ENST00000469391.5:c.4969C=	ENSP00000419438.1:p.Pro1657=
ENST00000495184.5:n.7224C=
NM_001190458.1:c.4969C=	NP_001177387.1:p.Pro1657=
NM_001193536.1:c.5065C=	NP_001180465.1:p.Pro1689=
NM_203447.3:c.5269C= , LRG_196t1:c.5269C=	NP_982272.2:p.Pro1757=
XM_011518045.1:c.4969C=	XP_011516347.1:p.Pro1657=
XM_011518046.1:c.5131C=	XP_011516348.1:p.Pro1711=
XM_011518047.1:c.5065C=	XP_011516349.1:p.Pro1689=
XM_011518048.1:c.5065C=	XP_011516350.1:p.Pro1689=
XM_011518049.1:c.3505C=	XP_011516351.1:p.Pro1169=
XM_011518045.3:c.4969C=	XP_011516347.1:p.Pro1657=
XM_011518046.2:c.5131C=	XP_011516348.1:p.Pro1711=
XM_011518047.3:c.5065C=	XP_011516349.1:p.Pro1689=
XM_011518048.2:c.5065C=	XP_011516350.1:p.Pro1689=
XM_011518049.2:c.3505C=	XP_011516351.1:p.Pro1169=
XM_017015173.1:c.5065C=	XP_016870662.1:p.Pro1689=
XM_017015174.1:c.5131C=	XP_016870663.1:p.Pro1711=
NM_001190458.2:c.4969C=	NP_001177387.1:p.Pro1657=
NM_001193536.2:c.5065C=	NP_001180465.1:p.Pro1689=
NM_203447.4:c.5269C= MANE Select	NP_982272.2:p.Pro1757=