Canonical Allele Identifier: CA1206550532
Gene: GORAB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.170539422A= , CM000663.2:g.170539422A= GRCh38
NC_000001.10:g.170508563A= , CM000663.1:g.170508563A= GRCh37
NC_000001.9:g.168775187A= NCBI36
NG_012237.1:g.12301A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684929.1:n.243A=
ENST00000685515.1:c.*138A= ENSP00000509073.1:n.*138A=
ENST00000685976.1:n.379A=
ENST00000686135.1:n.1734A=
ENST00000686870.1:c.274A= ENSP00000510121.1:p.Thr92=
ENST00000687370.1:n.3290A=
ENST00000687880.1:c.*268A= ENSP00000508486.1:n.*268A=
ENST00000688499.1:c.*138A= ENSP00000509581.1:n.*138A=
ENST00000688688.1:c.223A= ENSP00000510426.1:p.Thr75=
ENST00000689173.1:c.*268A= ENSP00000509341.1:n.*268A=
ENST00000690124.1:n.438A=
ENST00000690898.1:n.463A=
ENST00000691199.1:n.191-3069A=
ENST00000691235.1:n.139-3069A=
ENST00000691574.1:n.308A=
ENST00000692234.1:c.*138A= ENSP00000508508.1:n.*138A=
ENST00000692855.1:n.425A=
ENST00000692875.1:c.223A= ENSP00000508785.1:p.Thr75=
ENST00000693173.1:c.*268A= ENSP00000510143.1:n.*268A=
ENST00000693373.1:n.262A=
ENST00000367762.2:c.274A= ENSP00000356736.2:p.Thr92=
ENST00000367763.8:c.274A= MANE Select ENSP00000356737.4:p.Thr92=
ENST00000498166.6:c.*268A= ENSP00000473336.2:n.*268A=
ENST00000367762.1:c.349A= ENSP00000356736.1:p.Thr117=
ENST00000367763.7:c.349A= ENSP00000356737.3:p.Thr117=
ENST00000465717.1:n.360A=
ENST00000498166.5:c.647A=
ENST00000498600.2:n.361A=
NM_001146039.1:c.349A= NP_001139511.1:p.Thr117=
NM_152281.2:c.349A= NP_689494.2:p.Thr117=
NR_027397.1:n.376A=
XM_006711628.2:c.-196A= XP_006711691.1:n.-196A=
XM_006711629.2:c.-192A= XP_006711692.1:n.-192A=
XM_011510149.1:c.298A= XP_011508451.1:p.Thr100=
XM_011510150.1:c.-196A= XP_011508452.1:n.-196A=
XM_011510151.1:c.-196A= XP_011508453.1:n.-196A=
NM_001320252.1:c.-192A= NP_001307181.1:n.-192A=
XM_006711628.4:c.-196A= XP_006711691.1:n.-196A=
XM_011510149.2:c.298A= XP_011508451.1:p.Thr100=
XM_011510150.3:c.-196A= XP_011508452.1:n.-196A=
XM_017002807.1:c.-196A= XP_016858296.1:n.-196A=
XM_024450864.1:c.-192A= XP_024306632.1:n.-192A=
NM_001146039.2:c.274A= NP_001139511.2:p.Thr92=
NM_001320252.2:c.-192A= NP_001307181.1:n.-192A=
NM_152281.3:c.274A= MANE Select NP_689494.3:p.Thr92=
NR_027397.2:n.332A=