Canonical Allele Identifier: CA1148224357

Gene: DOCK7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.62457653C= , CM000663.2:g.62457653C=	GRCh38
NC_000001.10:g.62923324C= , CM000663.1:g.62923324C=	GRCh37
NC_000001.9:g.62695912C=	NCBI36
NG_033073.1:g.235716G=
NG_033073.2:g.235716G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001367561.1:c.6265G= MANE Select	NP_001354490.1:p.Glu2089=
ENST00000635253.2:c.6265G= MANE Select	ENSP00000489124.1:p.Glu2089=
NM_001271999.1:c.6232G=	NP_001258928.1:p.Glu2078=
NM_001271999.2:c.6232G=	NP_001258928.1:p.Glu2078=
NM_001272000.1:c.6145G=	NP_001258929.1:p.Glu2049=
NM_001272000.2:c.6145G=	NP_001258929.1:p.Glu2049=
NM_001272001.1:c.6139G=	NP_001258930.1:p.Glu2047=
NM_001272001.2:c.6139G=	NP_001258930.1:p.Glu2047=
NM_001330614.1:c.6238G=	NP_001317543.1:p.Glu2080=
NM_001330614.2:c.6238G=	NP_001317543.1:p.Glu2080=
NM_033407.3:c.6172G=	NP_212132.2:p.Glu2058=
NM_033407.4:c.6172G=	NP_212132.2:p.Glu2058=
ENST00000251157.10:c.6238G=	ENSP00000251157.6:p.Glu2080=
ENST00000340370.10:c.6172G=	ENSP00000340742.5:p.Glu2058=
ENST00000454575.6:c.6232G=	ENSP00000413583.2:p.Glu2078=
ENST00000634264.1:c.6145G=	ENSP00000489284.1:p.Glu2049=
ENST00000634495.1:n.951G=
ENST00000634495.2:n.2406G=
ENST00000635123.1:c.6139G=	ENSP00000489499.1:p.Glu2047=
ENST00000635253.1:c.6265G=	ENSP00000489124.1:p.Glu2089=
ENST00000635348.1:n.1547G=
ENST00000635983.1:n.5944G=
ENST00000637255.1:c.3532G=	ENSP00000490888.1:p.Glu1178=
XM_005271292.1:c.6238G=	XP_005271349.1:p.Glu2080=
XM_011542326.1:c.6265G=	XP_011540628.1:p.Glu2089=
XM_011542326.2:c.6265G=	XP_011540628.1:p.Glu2089=
XM_011542327.1:c.6259G=	XP_011540629.1:p.Glu2087=
XM_011542327.2:c.6259G=	XP_011540629.1:p.Glu2087=
XM_011542328.1:c.6250G=	XP_011540630.1:p.Glu2084=
XM_011542328.2:c.6250G=	XP_011540630.1:p.Glu2084=
XM_017002639.1:c.6166G=	XP_016858128.1:p.Glu2056=