Canonical Allele Identifier: CA343162974

Gene: GORAB

Linked Data

• MyVariant Identifiers: chr1:g.170508663T>A (hg19) ; chr1:g.170539522T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.170539522T>A , CM000663.2:g.170539522T>A	GRCh38
NC_000001.10:g.170508663T>A , CM000663.1:g.170508663T>A	GRCh37
NC_000001.9:g.168775287T>A	NCBI36
NG_012237.1:g.12401T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684929.1:n.343T>A
ENST00000685515.1:c.*238T>A	ENSP00000509073.1:n.*238T>A
ENST00000685976.1:n.479T>A
ENST00000686135.1:n.1834T>A
ENST00000686870.1:c.374T>A	ENSP00000510121.1:p.Leu125Gln
ENST00000687370.1:n.3390T>A
ENST00000687880.1:c.*368T>A	ENSP00000508486.1:n.*368T>A
ENST00000688499.1:c.*238T>A	ENSP00000509581.1:n.*238T>A
ENST00000688688.1:c.323T>A	ENSP00000510426.1:p.Leu108Gln
ENST00000689173.1:c.*368T>A	ENSP00000509341.1:n.*368T>A
ENST00000690124.1:n.538T>A
ENST00000690898.1:n.563T>A
ENST00000691199.1:n.191-2969T>A
ENST00000691235.1:n.139-2969T>A
ENST00000691574.1:n.408T>A
ENST00000692234.1:c.*238T>A	ENSP00000508508.1:n.*238T>A
ENST00000692855.1:n.525T>A
ENST00000692875.1:c.323T>A	ENSP00000508785.1:p.Leu108Gln
ENST00000693173.1:c.*368T>A	ENSP00000510143.1:n.*368T>A
ENST00000693373.1:n.362T>A
ENST00000367762.2:c.374T>A	ENSP00000356736.2:p.Leu125Gln
ENST00000367763.8:c.374T>A MANE Select	ENSP00000356737.4:p.Leu125Gln
ENST00000498166.6:c.*368T>A	ENSP00000473336.2:n.*368T>A
ENST00000367762.1:c.449T>A	ENSP00000356736.1:p.Leu150Gln
ENST00000367763.7:c.449T>A	ENSP00000356737.3:p.Leu150Gln
ENST00000465717.1:n.460T>A
ENST00000498166.5:c.747T>A
ENST00000498600.2:n.461T>A
NM_001146039.1:c.449T>A	NP_001139511.1:p.Leu150Gln
NM_152281.2:c.449T>A	NP_689494.2:p.Leu150Gln
NR_027397.1:n.476T>A
XM_006711628.2:c.-96T>A	XP_006711691.1:n.-96T>A
XM_006711629.2:c.-92T>A	XP_006711692.1:n.-92T>A
XM_011510149.1:c.398T>A	XP_011508451.1:p.Leu133Gln
XM_011510150.1:c.-96T>A	XP_011508452.1:n.-96T>A
XM_011510151.1:c.-96T>A	XP_011508453.1:n.-96T>A
NM_001320252.1:c.-92T>A	NP_001307181.1:n.-92T>A
XM_006711628.4:c.-96T>A	XP_006711691.1:n.-96T>A
XM_011510149.2:c.398T>A	XP_011508451.1:p.Leu133Gln
XM_011510150.3:c.-96T>A	XP_011508452.1:n.-96T>A
XM_017002807.1:c.-96T>A	XP_016858296.1:n.-96T>A
XM_024450864.1:c.-92T>A	XP_024306632.1:n.-92T>A
NM_001146039.2:c.374T>A	NP_001139511.2:p.Leu125Gln
NM_001320252.2:c.-92T>A	NP_001307181.1:n.-92T>A
NM_152281.3:c.374T>A MANE Select	NP_689494.3:p.Leu125Gln
NR_027397.2:n.432T>A