Canonical Allele Identifier: CA1826888987

Gene: DOCK8

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.414810A= , CM000671.2:g.414810A=	GRCh38
NC_000009.11:g.414810A= , CM000671.1:g.414810A=	GRCh37
NC_000009.10:g.404810A=	NCBI36
NG_017007.1:g.204946A= , LRG_196:g.204946A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382329.2:c.3259A=	ENSP00000371766.2:p.Ser1087=
ENST00000683406.1:n.80A=
ENST00000685949.1:n.2347A=
ENST00000432829.7:c.3559A= MANE Select	ENSP00000394888.3:p.Ser1187=
ENST00000382329.1:c.1960A=	ENSP00000371766.1:p.Ser654=
ENST00000432829.6:c.3559A=	ENSP00000394888.3:p.Ser1187=
ENST00000453981.5:c.3355A=	ENSP00000408464.2:p.Ser1119=
ENST00000469391.5:c.3259A=	ENSP00000419438.1:p.Ser1087=
ENST00000495184.5:n.5514A=
NM_001190458.1:c.3259A=	NP_001177387.1:p.Ser1087=
NM_001193536.1:c.3355A=	NP_001180465.1:p.Ser1119=
NM_203447.3:c.3559A= , LRG_196t1:c.3559A=	NP_982272.2:p.Ser1187=
XM_011518045.1:c.3259A=	XP_011516347.1:p.Ser1087=
XM_011518046.1:c.3421A=	XP_011516348.1:p.Ser1141=
XM_011518047.1:c.3355A=	XP_011516349.1:p.Ser1119=
XM_011518048.1:c.3355A=	XP_011516350.1:p.Ser1119=
XM_011518049.1:c.1795A=	XP_011516351.1:p.Ser599=
XM_011518045.3:c.3259A=	XP_011516347.1:p.Ser1087=
XM_011518046.2:c.3421A=	XP_011516348.1:p.Ser1141=
XM_011518047.3:c.3355A=	XP_011516349.1:p.Ser1119=
XM_011518048.2:c.3355A=	XP_011516350.1:p.Ser1119=
XM_011518049.2:c.1795A=	XP_011516351.1:p.Ser599=
XM_017015173.1:c.3355A=	XP_016870662.1:p.Ser1119=
XM_017015174.1:c.3421A=	XP_016870663.1:p.Ser1141=
NM_001190458.2:c.3259A=	NP_001177387.1:p.Ser1087=
NM_001193536.2:c.3355A=	NP_001180465.1:p.Ser1119=
NM_203447.4:c.3559A= MANE Select	NP_982272.2:p.Ser1187=