Canonical Allele Identifier: CA10511978

Gene: OCRL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129548598A>G , CM000685.2:g.129548598A>G	GRCh38
NC_000023.10:g.128682575A>G , CM000685.1:g.128682575A>G	GRCh37
NC_000023.9:g.128510256A>G	NCBI36
NG_008638.1:g.13324A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000276.4:c.235A>G MANE Select	NP_000267.2:p.Asn79Asp
ENST00000371113.9:c.235A>G MANE Select	ENSP00000360154.4:p.Asn79Asp
NM_000276.3:c.235A>G	NP_000267.2:p.Asn79Asp
NM_001318784.1:c.238A>G	NP_001305713.1:p.Asn80Asp
NM_001318784.2:c.238A>G	NP_001305713.1:p.Asn80Asp
NM_001587.3:c.235A>G	NP_001578.2:p.Asn79Asp
NM_001587.4:c.235A>G	NP_001578.2:p.Asn79Asp
ENST00000357121.5:c.235A>G	ENSP00000349635.5:p.Asn79Asp
ENST00000371113.8:c.235A>G	ENSP00000360154.4:p.Asn79Asp
ENST00000486673.1:n.207A>G
ENST00000646010.1:c.192A>G
ENST00000689093.1:c.101A>G
ENST00000691455.1:c.*527A>G	ENSP00000510265.1:n.*527A>G
ENST00000693473.1:c.192A>G
XM_005262422.1:c.-237A>G	XP_005262479.1:n.-237A>G
XM_005262422.2:c.-237A>G	XP_005262479.1:n.-237A>G
XM_011531342.1:c.238A>G	XP_011529644.1:p.Asn80Asp
XM_011531343.1:c.238A>G	XP_011529645.1:p.Asn80Asp
XM_011531344.1:c.-31A>G	XP_011529646.1:n.-31A>G
XM_011531344.3:c.-31A>G	XP_011529646.1:n.-31A>G
XM_011531345.1:c.-31A>G	XP_011529647.1:n.-31A>G
XM_011531345.3:c.-31A>G	XP_011529647.1:n.-31A>G
XM_011531346.1:c.238A>G	XP_011529648.1:p.Asn80Asp
XM_017029554.1:c.235A>G	XP_016885043.1:p.Asn79Asp