Canonical Allele Identifier: CA1206550529
Gene: GORAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.170539421C= , CM000663.2:g.170539421C= GRCh38
NC_000001.10:g.170508562C= , CM000663.1:g.170508562C= GRCh37
NC_000001.9:g.168775186C= NCBI36
NG_012237.1:g.12300C=

Transcript Alleles

HGVS Amino-acid change
ENST00000684929.1:n.242C=
ENST00000685515.1:c.*137C= ENSP00000509073.1:n.*137C=
ENST00000685976.1:n.378C=
ENST00000686135.1:n.1733C=
ENST00000686870.1:c.273C= ENSP00000510121.1:p.Leu91=
ENST00000687370.1:n.3289C=
ENST00000687880.1:c.*267C= ENSP00000508486.1:n.*267C=
ENST00000688499.1:c.*137C= ENSP00000509581.1:n.*137C=
ENST00000688688.1:c.222C= ENSP00000510426.1:p.Leu74=
ENST00000689173.1:c.*267C= ENSP00000509341.1:n.*267C=
ENST00000690124.1:n.437C=
ENST00000690898.1:n.462C=
ENST00000691199.1:n.191-3070C=
ENST00000691235.1:n.139-3070C=
ENST00000691574.1:n.307C=
ENST00000692234.1:c.*137C= ENSP00000508508.1:n.*137C=
ENST00000692855.1:n.424C=
ENST00000692875.1:c.222C= ENSP00000508785.1:p.Leu74=
ENST00000693173.1:c.*267C= ENSP00000510143.1:n.*267C=
ENST00000693373.1:n.261C=
ENST00000367762.2:c.273C= ENSP00000356736.2:p.Leu91=
ENST00000367763.8:c.273C= MANE Select ENSP00000356737.4:p.Leu91=
ENST00000498166.6:c.*267C= ENSP00000473336.2:n.*267C=
ENST00000367762.1:c.348C= ENSP00000356736.1:p.Leu116=
ENST00000367763.7:c.348C= ENSP00000356737.3:p.Leu116=
ENST00000465717.1:n.359C=
ENST00000498166.5:c.646C=
ENST00000498600.2:n.360C=
NM_001146039.1:c.348C= NP_001139511.1:p.Leu116=
NM_152281.2:c.348C= NP_689494.2:p.Leu116=
NR_027397.1:n.375C=
XM_006711628.2:c.-197C= XP_006711691.1:n.-197C=
XM_006711629.2:c.-193C= XP_006711692.1:n.-193C=
XM_011510149.1:c.297C= XP_011508451.1:p.Leu99=
XM_011510150.1:c.-197C= XP_011508452.1:n.-197C=
XM_011510151.1:c.-197C= XP_011508453.1:n.-197C=
NM_001320252.1:c.-193C= NP_001307181.1:n.-193C=
XM_006711628.4:c.-197C= XP_006711691.1:n.-197C=
XM_011510149.2:c.297C= XP_011508451.1:p.Leu99=
XM_011510150.3:c.-197C= XP_011508452.1:n.-197C=
XM_017002807.1:c.-197C= XP_016858296.1:n.-197C=
XM_024450864.1:c.-193C= XP_024306632.1:n.-193C=
NM_001146039.2:c.273C= NP_001139511.2:p.Leu91=
NM_001320252.2:c.-193C= NP_001307181.1:n.-193C=
NM_152281.3:c.273C= MANE Select NP_689494.3:p.Leu91=
NR_027397.2:n.331C=