Canonical Allele Identifier: CA2458108095
Gene: OCRL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.129589908G= , CM000685.2:g.129589908G= GRCh38
NC_000023.10:g.128723885G= , CM000685.1:g.128723885G= GRCh37
NC_000023.9:g.128551566G= NCBI36
NG_008638.1:g.54634G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000693473.1:c.2650G=
ENST00000371113.9:c.2533G= MANE Select ENSP00000360154.4:p.Glu845=
ENST00000646010.1:c.2581G=
ENST00000646914.1:c.1838G=
ENST00000647245.1:c.2084G=
ENST00000357121.5:c.2509G= ENSP00000349635.5:p.Glu837=
ENST00000371113.8:c.2533G= ENSP00000360154.4:p.Glu845=
ENST00000463271.1:n.320G=
NM_000276.3:c.2533G= NP_000267.2:p.Glu845=
NM_001587.3:c.2509G= NP_001578.2:p.Glu837=
XM_005262422.1:c.2062G= XP_005262479.1:p.Glu688=
XM_011531342.1:c.2536G= XP_011529644.1:p.Glu846=
XM_011531343.1:c.2512G= XP_011529645.1:p.Glu838=
XM_011531344.1:c.2389G= XP_011529646.1:p.Glu797=
XM_011531345.1:c.2389G= XP_011529647.1:p.Glu797=
NM_001318784.1:c.2536G= NP_001305713.1:p.Glu846=
XM_005262422.2:c.2062G= XP_005262479.1:p.Glu688=
XM_011531344.3:c.2389G= XP_011529646.1:p.Glu797=
XM_011531345.3:c.2389G= XP_011529647.1:p.Glu797=
NM_000276.4:c.2533G= MANE Select NP_000267.2:p.Glu845=
NM_001318784.2:c.2536G= NP_001305713.1:p.Glu846=
NM_001587.4:c.2509G= NP_001578.2:p.Glu837=