Canonical Allele Identifier: CA335708156

Gene: OCRL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129587339T>C , CM000685.2:g.129587339T>C	GRCh38
NC_000023.10:g.128721316T>C , CM000685.1:g.128721316T>C	GRCh37
NC_000023.9:g.128548997T>C	NCBI36
NG_008638.1:g.52065T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000276.4:c.2256+221T>C MANE Select	NP_000267.2:n.2256+221T>C
ENST00000371113.9:c.2256+221T>C MANE Select	ENSP00000360154.4:n.2256+221T>C
NM_000276.3:c.2256+221T>C	NP_000267.2:n.2256+221T>C
NM_001318784.1:c.2259+221T>C	NP_001305713.1:n.2259+221T>C
NM_001318784.2:c.2259+221T>C	NP_001305713.1:n.2259+221T>C
NM_001587.3:c.2232+221T>C	NP_001578.2:n.2232+221T>C
NM_001587.4:c.2232+221T>C	NP_001578.2:n.2232+221T>C
ENST00000357121.5:c.2232+221T>C	ENSP00000349635.5:n.2232+221T>C
ENST00000371113.8:c.2256+221T>C	ENSP00000360154.4:n.2256+221T>C
ENST00000646010.1:c.2304+221T>C
ENST00000646914.1:c.1433+221T>C
ENST00000647245.1:c.1807+221T>C
ENST00000693473.1:c.2373+221T>C
XM_005262422.1:c.1785+221T>C	XP_005262479.1:n.1785+221T>C
XM_005262422.2:c.1785+221T>C	XP_005262479.1:n.1785+221T>C
XM_011531342.1:c.2259+221T>C	XP_011529644.1:n.2259+221T>C
XM_011531343.1:c.2235+221T>C	XP_011529645.1:n.2235+221T>C
XM_011531344.1:c.2112+221T>C	XP_011529646.1:n.2112+221T>C
XM_011531344.3:c.2112+221T>C	XP_011529646.1:n.2112+221T>C
XM_011531345.1:c.2112+221T>C	XP_011529647.1:n.2112+221T>C
XM_011531345.3:c.2112+221T>C	XP_011529647.1:n.2112+221T>C
XM_011531346.1:c.2259+221T>C	XP_011529648.1:n.2259+221T>C
XM_017029554.1:c.2256+221T>C	XP_016885043.1:n.2256+221T>C