Canonical Allele Identifier: CA2458108094

Gene: OCRL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129589906G= , CM000685.2:g.129589906G=	GRCh38
NC_000023.10:g.128723883G= , CM000685.1:g.128723883G=	GRCh37
NC_000023.9:g.128551564G=	NCBI36
NG_008638.1:g.54632G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000693473.1:c.2648G=
ENST00000371113.9:c.2531G= MANE Select	ENSP00000360154.4:p.Arg844=
ENST00000646010.1:c.2579G=
ENST00000646914.1:c.1836G=
ENST00000647245.1:c.2082G=
ENST00000357121.5:c.2507G=	ENSP00000349635.5:p.Arg836=
ENST00000371113.8:c.2531G=	ENSP00000360154.4:p.Arg844=
ENST00000463271.1:n.318G=
NM_000276.3:c.2531G=	NP_000267.2:p.Arg844=
NM_001587.3:c.2507G=	NP_001578.2:p.Arg836=
XM_005262422.1:c.2060G=	XP_005262479.1:p.Arg687=
XM_011531342.1:c.2534G=	XP_011529644.1:p.Arg845=
XM_011531343.1:c.2510G=	XP_011529645.1:p.Arg837=
XM_011531344.1:c.2387G=	XP_011529646.1:p.Arg796=
XM_011531345.1:c.2387G=	XP_011529647.1:p.Arg796=
NM_001318784.1:c.2534G=	NP_001305713.1:p.Arg845=
XM_005262422.2:c.2060G=	XP_005262479.1:p.Arg687=
XM_011531344.3:c.2387G=	XP_011529646.1:p.Arg796=
XM_011531345.3:c.2387G=	XP_011529647.1:p.Arg796=
NM_000276.4:c.2531G= MANE Select	NP_000267.2:p.Arg844=
NM_001318784.2:c.2534G=	NP_001305713.1:p.Arg845=
NM_001587.4:c.2507G=	NP_001578.2:p.Arg836=