Canonical Allele Identifier: CA1148224363

Gene: DOCK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62529349G= , CM000663.2:g.62529349G=	GRCh38
NC_000001.10:g.62995020G= , CM000663.1:g.62995020G=	GRCh37
NC_000001.9:g.62767608G=	NCBI36
NG_033073.1:g.164020C=
NG_033073.2:g.164020C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635253.2:c.3709C= MANE Select	ENSP00000489124.1:p.Arg1237=
ENST00000637208.1:c.*1829C=	ENSP00000490079.1:n.*1829C=
ENST00000637255.1:c.1009C=	ENSP00000490888.1:p.Arg337=
ENST00000251157.10:c.3709C=	ENSP00000251157.6:p.Arg1237=
ENST00000340370.10:c.3616C=	ENSP00000340742.5:p.Arg1206=
ENST00000454575.6:c.3709C=	ENSP00000413583.2:p.Arg1237=
ENST00000634264.1:c.3616C=	ENSP00000489284.1:p.Arg1206=
ENST00000635123.1:c.3616C=	ENSP00000489499.1:p.Arg1206=
ENST00000635253.1:c.3709C=	ENSP00000489124.1:p.Arg1237=
NM_001271999.1:c.3709C=	NP_001258928.1:p.Arg1237=
NM_001272000.1:c.3616C=	NP_001258929.1:p.Arg1206=
NM_001272001.1:c.3616C=	NP_001258930.1:p.Arg1206=
NM_033407.3:c.3616C=	NP_212132.2:p.Arg1206=
XM_005271292.1:c.3709C=	XP_005271349.1:p.Arg1237=
XM_011542326.1:c.3709C=	XP_011540628.1:p.Arg1237=
XM_011542327.1:c.3709C=	XP_011540629.1:p.Arg1237=
XM_011542328.1:c.3709C=	XP_011540630.1:p.Arg1237=
XM_011542329.1:c.3709C=	XP_011540631.1:p.Arg1237=
XM_011542330.1:c.3709C=	XP_011540632.1:p.Arg1237=
NM_001330614.1:c.3709C=	NP_001317543.1:p.Arg1237=
XM_011542326.2:c.3709C=	XP_011540628.1:p.Arg1237=
XM_011542327.2:c.3709C=	XP_011540629.1:p.Arg1237=
XM_011542328.2:c.3709C=	XP_011540630.1:p.Arg1237=
XM_011542330.2:c.3709C=	XP_011540632.1:p.Arg1237=
XM_017002639.1:c.3616C=	XP_016858128.1:p.Arg1206=
XM_017002640.1:c.3709C=	XP_016858129.1:p.Arg1237=
NM_001367561.1:c.3709C= MANE Select	NP_001354490.1:p.Arg1237=
NM_001271999.2:c.3709C=	NP_001258928.1:p.Arg1237=
NM_001272000.2:c.3616C=	NP_001258929.1:p.Arg1206=
NM_001272001.2:c.3616C=	NP_001258930.1:p.Arg1206=
NM_001330614.2:c.3709C=	NP_001317543.1:p.Arg1237=
NM_033407.4:c.3616C=	NP_212132.2:p.Arg1206=