Canonical Allele Identifier: CA414551332

Gene: OCRL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129558667G>T , CM000685.2:g.129558667G>T	GRCh38
NC_000023.10:g.128692644G>T , CM000685.1:g.128692644G>T	GRCh37
NC_000023.9:g.128520325G>T	NCBI36
NG_008638.1:g.23393G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000276.4:c.474G>T MANE Select	NP_000267.2:p.Met158Ile
ENST00000371113.9:c.474G>T MANE Select	ENSP00000360154.4:p.Met158Ile
NM_000276.3:c.474G>T	NP_000267.2:p.Met158Ile
NM_001318784.1:c.477G>T	NP_001305713.1:p.Met159Ile
NM_001318784.2:c.477G>T	NP_001305713.1:p.Met159Ile
NM_001587.3:c.474G>T	NP_001578.2:p.Met158Ile
NM_001587.4:c.474G>T	NP_001578.2:p.Met158Ile
ENST00000357121.5:c.474G>T	ENSP00000349635.5:p.Met158Ile
ENST00000371113.8:c.474G>T	ENSP00000360154.4:p.Met158Ile
ENST00000486673.1:n.716G>T
ENST00000646010.1:c.522G>T
ENST00000647245.1:c.125G>T
ENST00000689093.1:c.1551G>T
ENST00000691455.1:c.*766G>T	ENSP00000510265.1:n.*766G>T
ENST00000693473.1:c.591G>T
XM_005262422.1:c.3G>T	XP_005262479.1:p.Met1Ile
XM_005262422.2:c.3G>T	XP_005262479.1:p.Met1Ile
XM_011531342.1:c.477G>T	XP_011529644.1:p.Met159Ile
XM_011531343.1:c.477G>T	XP_011529645.1:p.Met159Ile
XM_011531344.1:c.330G>T	XP_011529646.1:p.Met110Ile
XM_011531344.3:c.330G>T	XP_011529646.1:p.Met110Ile
XM_011531345.1:c.330G>T	XP_011529647.1:p.Met110Ile
XM_011531345.3:c.330G>T	XP_011529647.1:p.Met110Ile
XM_011531346.1:c.477G>T	XP_011529648.1:p.Met159Ile
XM_017029554.1:c.474G>T	XP_016885043.1:p.Met158Ile