Canonical Allele Identifier: CA414616455

Gene: OCRL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129569338G>A , CM000685.2:g.129569338G>A	GRCh38
NC_000023.10:g.128703315G>A , CM000685.1:g.128703315G>A	GRCh37
NC_000023.9:g.128530996G>A	NCBI36
NG_008638.1:g.34064G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000276.4:c.1541G>A MANE Select	NP_000267.2:p.Arg514Gln
ENST00000371113.9:c.1541G>A MANE Select	ENSP00000360154.4:p.Arg514Gln
NM_000276.3:c.1541G>A	NP_000267.2:p.Arg514Gln
NM_001318784.1:c.1544G>A	NP_001305713.1:p.Arg515Gln
NM_001318784.2:c.1544G>A	NP_001305713.1:p.Arg515Gln
NM_001587.3:c.1541G>A	NP_001578.2:p.Arg514Gln
NM_001587.4:c.1541G>A	NP_001578.2:p.Arg514Gln
ENST00000357121.5:c.1541G>A	ENSP00000349635.5:p.Arg514Gln
ENST00000371113.8:c.1541G>A	ENSP00000360154.4:p.Arg514Gln
ENST00000646010.1:c.1589G>A
ENST00000646914.1:c.652G>A
ENST00000647245.1:c.1192G>A
ENST00000691455.1:c.*1833G>A	ENSP00000510265.1:n.*1833G>A
ENST00000693473.1:c.1658G>A
XM_005262422.1:c.1070G>A	XP_005262479.1:p.Arg357Gln
XM_005262422.2:c.1070G>A	XP_005262479.1:p.Arg357Gln
XM_011531342.1:c.1544G>A	XP_011529644.1:p.Arg515Gln
XM_011531343.1:c.1544G>A	XP_011529645.1:p.Arg515Gln
XM_011531344.1:c.1397G>A	XP_011529646.1:p.Arg466Gln
XM_011531344.3:c.1397G>A	XP_011529646.1:p.Arg466Gln
XM_011531345.1:c.1397G>A	XP_011529647.1:p.Arg466Gln
XM_011531345.3:c.1397G>A	XP_011529647.1:p.Arg466Gln
XM_011531346.1:c.1544G>A	XP_011529648.1:p.Arg515Gln
XM_017029554.1:c.1541G>A	XP_016885043.1:p.Arg514Gln