Canonical Allele Identifier: CA414551899

Gene: OCRL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129559001G>C , CM000685.2:g.129559001G>C	GRCh38
NC_000023.10:g.128692978G>C , CM000685.1:g.128692978G>C	GRCh37
NC_000023.9:g.128520659G>C	NCBI36
NG_008638.1:g.23727G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000276.4:c.722G>C MANE Select	NP_000267.2:p.Arg241Thr
ENST00000371113.9:c.722G>C MANE Select	ENSP00000360154.4:p.Arg241Thr
NM_000276.3:c.722G>C	NP_000267.2:p.Arg241Thr
NM_001318784.1:c.725G>C	NP_001305713.1:p.Arg242Thr
NM_001318784.2:c.725G>C	NP_001305713.1:p.Arg242Thr
NM_001587.3:c.722G>C	NP_001578.2:p.Arg241Thr
NM_001587.4:c.722G>C	NP_001578.2:p.Arg241Thr
ENST00000357121.5:c.722G>C	ENSP00000349635.5:p.Arg241Thr
ENST00000371113.8:c.722G>C	ENSP00000360154.4:p.Arg241Thr
ENST00000646010.1:c.770G>C
ENST00000647245.1:c.373G>C
ENST00000691455.1:c.*1014G>C	ENSP00000510265.1:n.*1014G>C
ENST00000693473.1:c.839G>C
XM_005262422.1:c.251G>C	XP_005262479.1:p.Arg84Thr
XM_005262422.2:c.251G>C	XP_005262479.1:p.Arg84Thr
XM_011531342.1:c.725G>C	XP_011529644.1:p.Arg242Thr
XM_011531343.1:c.725G>C	XP_011529645.1:p.Arg242Thr
XM_011531344.1:c.578G>C	XP_011529646.1:p.Arg193Thr
XM_011531344.3:c.578G>C	XP_011529646.1:p.Arg193Thr
XM_011531345.1:c.578G>C	XP_011529647.1:p.Arg193Thr
XM_011531345.3:c.578G>C	XP_011529647.1:p.Arg193Thr
XM_011531346.1:c.725G>C	XP_011529648.1:p.Arg242Thr
XM_017029554.1:c.722G>C	XP_016885043.1:p.Arg241Thr