Canonical Allele Identifier: CA2458108096
Gene: OCRL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.129589915T= , CM000685.2:g.129589915T= GRCh38
NC_000023.10:g.128723892T= , CM000685.1:g.128723892T= GRCh37
NC_000023.9:g.128551573T= NCBI36
NG_008638.1:g.54641T=

Transcript Alleles

HGVS Amino-acid change
ENST00000693473.1:c.2657T=
ENST00000371113.9:c.2540T= MANE Select ENSP00000360154.4:p.Leu847=
ENST00000646010.1:c.2588T=
ENST00000646914.1:c.1845T=
ENST00000647245.1:c.2091T=
ENST00000357121.5:c.2516T= ENSP00000349635.5:p.Leu839=
ENST00000371113.8:c.2540T= ENSP00000360154.4:p.Leu847=
ENST00000463271.1:n.327T=
NM_000276.3:c.2540T= NP_000267.2:p.Leu847=
NM_001587.3:c.2516T= NP_001578.2:p.Leu839=
XM_005262422.1:c.2069T= XP_005262479.1:p.Leu690=
XM_011531342.1:c.2543T= XP_011529644.1:p.Leu848=
XM_011531343.1:c.2519T= XP_011529645.1:p.Leu840=
XM_011531344.1:c.2396T= XP_011529646.1:p.Leu799=
XM_011531345.1:c.2396T= XP_011529647.1:p.Leu799=
NM_001318784.1:c.2543T= NP_001305713.1:p.Leu848=
XM_005262422.2:c.2069T= XP_005262479.1:p.Leu690=
XM_011531344.3:c.2396T= XP_011529646.1:p.Leu799=
XM_011531345.3:c.2396T= XP_011529647.1:p.Leu799=
NM_000276.4:c.2540T= MANE Select NP_000267.2:p.Leu847=
NM_001318784.2:c.2543T= NP_001305713.1:p.Leu848=
NM_001587.4:c.2516T= NP_001578.2:p.Leu839=