Canonical Allele Identifier: CA414621105

Gene: OCRL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129576416A>C , CM000685.2:g.129576416A>C	GRCh38
NC_000023.10:g.128710393A>C , CM000685.1:g.128710393A>C	GRCh37
NC_000023.9:g.128538074A>C	NCBI36
NG_008638.1:g.41142A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000276.4:c.1979A>C MANE Select	NP_000267.2:p.His660Pro
ENST00000371113.9:c.1979A>C MANE Select	ENSP00000360154.4:p.His660Pro
NM_000276.3:c.1979A>C	NP_000267.2:p.His660Pro
NM_001318784.1:c.1982A>C	NP_001305713.1:p.His661Pro
NM_001318784.2:c.1982A>C	NP_001305713.1:p.His661Pro
NM_001587.3:c.1979A>C	NP_001578.2:p.His660Pro
NM_001587.4:c.1979A>C	NP_001578.2:p.His660Pro
ENST00000357121.5:c.1979A>C	ENSP00000349635.5:p.His660Pro
ENST00000371113.8:c.1979A>C	ENSP00000360154.4:p.His660Pro
ENST00000646010.1:c.2027A>C
ENST00000646914.1:c.1156A>C
ENST00000647245.1:c.1530A>C
ENST00000691455.1:c.*2271A>C	ENSP00000510265.1:n.*2271A>C
ENST00000693473.1:c.2096A>C
XM_005262422.1:c.1508A>C	XP_005262479.1:p.His503Pro
XM_005262422.2:c.1508A>C	XP_005262479.1:p.His503Pro
XM_011531342.1:c.1982A>C	XP_011529644.1:p.His661Pro
XM_011531343.1:c.1982A>C	XP_011529645.1:p.His661Pro
XM_011531344.1:c.1835A>C	XP_011529646.1:p.His612Pro
XM_011531344.3:c.1835A>C	XP_011529646.1:p.His612Pro
XM_011531345.1:c.1835A>C	XP_011529647.1:p.His612Pro
XM_011531345.3:c.1835A>C	XP_011529647.1:p.His612Pro
XM_011531346.1:c.1982A>C	XP_011529648.1:p.His661Pro
XM_017029554.1:c.1979A>C	XP_016885043.1:p.His660Pro