Canonical Allele Identifier: CA2694654613

Gene: OCRL

Linked Data

• gnomAD v4: X-129569442-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129569442T>C , CM000685.2:g.129569442T>C	GRCh38
NC_000023.10:g.128703419T>C , CM000685.1:g.128703419T>C	GRCh37
NC_000023.9:g.128531100T>C	NCBI36
NG_008638.1:g.34168T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691455.1:c.*1894+43T>C	ENSP00000510265.1:n.*1894+43T>C
ENST00000693473.1:c.1719+43T>C
ENST00000371113.9:c.1602+43T>C MANE Select	ENSP00000360154.4:n.1602+43T>C
ENST00000646010.1:c.1650+43T>C
ENST00000646914.1:c.713+43T>C
ENST00000647245.1:c.1253+43T>C
ENST00000357121.5:c.1602+43T>C	ENSP00000349635.5:n.1602+43T>C
ENST00000371113.8:c.1602+43T>C	ENSP00000360154.4:n.1602+43T>C
NM_000276.3:c.1602+43T>C	NP_000267.2:n.1602+43T>C
NM_001587.3:c.1602+43T>C	NP_001578.2:n.1602+43T>C
XM_005262422.1:c.1131+43T>C	XP_005262479.1:n.1131+43T>C
XM_011531342.1:c.1605+43T>C	XP_011529644.1:n.1605+43T>C
XM_011531343.1:c.1605+43T>C	XP_011529645.1:n.1605+43T>C
XM_011531344.1:c.1458+43T>C	XP_011529646.1:n.1458+43T>C
XM_011531345.1:c.1458+43T>C	XP_011529647.1:n.1458+43T>C
XM_011531346.1:c.1605+43T>C	XP_011529648.1:n.1605+43T>C
NM_001318784.1:c.1605+43T>C	NP_001305713.1:n.1605+43T>C
XM_005262422.2:c.1131+43T>C	XP_005262479.1:n.1131+43T>C
XM_011531344.3:c.1458+43T>C	XP_011529646.1:n.1458+43T>C
XM_011531345.3:c.1458+43T>C	XP_011529647.1:n.1458+43T>C
XM_017029554.1:c.1602+43T>C	XP_016885043.1:n.1602+43T>C
NM_000276.4:c.1602+43T>C MANE Select	NP_000267.2:n.1602+43T>C
NM_001318784.2:c.1605+43T>C	NP_001305713.1:n.1605+43T>C
NM_001587.4:c.1602+43T>C	NP_001578.2:n.1602+43T>C