Canonical Allele Identifier: CA421932957

Gene: GORAB

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.170539214A>G , CM000663.2:g.170539214A>G	GRCh38
NC_000001.10:g.170508355A>G , CM000663.1:g.170508355A>G	GRCh37
NC_000001.9:g.168774979A>G	NCBI36
NG_012237.1:g.12093A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_152281.3:c.66A>G MANE Select	NP_689494.3:p.Pro22=
ENST00000367763.8:c.66A>G MANE Select	ENSP00000356737.4:p.Pro22=
NM_001146039.1:c.141A>G	NP_001139511.1:p.Pro47=
NM_001146039.2:c.66A>G	NP_001139511.2:p.Pro22=
NM_001320252.1:c.-400A>G	NP_001307181.1:n.-400A>G
NM_001320252.2:c.-400A>G	NP_001307181.1:n.-400A>G
NM_152281.2:c.141A>G	NP_689494.2:p.Pro47=
NR_027397.1:n.168A>G
NR_027397.2:n.124A>G
ENST00000367762.1:c.141A>G	ENSP00000356736.1:p.Pro47=
ENST00000367762.2:c.66A>G	ENSP00000356736.2:p.Pro22=
ENST00000367763.7:c.141A>G	ENSP00000356737.3:p.Pro47=
ENST00000465717.1:n.152A>G
ENST00000498166.5:c.439A>G
ENST00000498166.6:c.*60A>G	ENSP00000473336.2:n.*60A>G
ENST00000498600.2:n.153A>G
ENST00000684929.1:n.35A>G
ENST00000685515.1:c.254A>G	ENSP00000509073.1:p.His85Arg
ENST00000685976.1:n.171A>G
ENST00000686135.1:n.1526A>G
ENST00000686870.1:c.66A>G	ENSP00000510121.1:p.Pro22=
ENST00000687370.1:n.3082A>G
ENST00000687880.1:c.*60A>G	ENSP00000508486.1:n.*60A>G
ENST00000688499.1:c.254A>G	ENSP00000509581.1:p.His85Arg
ENST00000688688.1:c.15A>G	ENSP00000510426.1:p.Pro5=
ENST00000689173.1:c.*60A>G	ENSP00000509341.1:n.*60A>G
ENST00000690124.1:n.230A>G
ENST00000690898.1:n.255A>G
ENST00000691199.1:n.191-3277A>G
ENST00000691235.1:n.139-3277A>G
ENST00000691574.1:n.100A>G
ENST00000692234.1:c.254A>G	ENSP00000508508.1:p.His85Arg
ENST00000692855.1:n.217A>G
ENST00000692875.1:c.15A>G	ENSP00000508785.1:p.Pro5=
ENST00000693173.1:c.*60A>G	ENSP00000510143.1:n.*60A>G
ENST00000693373.1:n.54A>G
XM_006711628.2:c.-404A>G	XP_006711691.1:n.-404A>G
XM_006711628.4:c.-404A>G	XP_006711691.1:n.-404A>G
XM_006711629.2:c.-400A>G	XP_006711692.1:n.-400A>G
XM_011510149.1:c.90A>G	XP_011508451.1:p.Pro30=
XM_011510149.2:c.90A>G	XP_011508451.1:p.Pro30=
XM_011510150.1:c.-404A>G	XP_011508452.1:n.-404A>G
XM_011510150.3:c.-404A>G	XP_011508452.1:n.-404A>G
XM_011510151.1:c.-404A>G	XP_011508453.1:n.-404A>G
XM_017002807.1:c.-404A>G	XP_016858296.1:n.-404A>G
XM_024450864.1:c.-400A>G	XP_024306632.1:n.-400A>G