Canonical Allele Identifier: CA266138

Gene: OCRL

Linked Data

• ClinVar Variation Id: 68695
• ClinVar RCV Id: RCV000059576 ; RCV003488373
• dbSNP Id: rs137853831
• gnomAD v2: X-128696430-C-T
• gnomAD v3: X-129562453-C-T
• gnomAD v4: X-129562453-C-T
• COSMIC: COSM6447736
• MyVariant Identifiers: chrX:g.128696430C>T (hg19) ; chrX:g.129562453C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129562453C>T , CM000685.2:g.129562453C>T	GRCh38
NC_000023.10:g.128696430C>T , CM000685.1:g.128696430C>T	GRCh37
NC_000023.9:g.128524111C>T	NCBI36
NG_008638.1:g.27179C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000691455.1:c.*1301C>T	ENSP00000510265.1:n.*1301C>T
ENST00000693473.1:c.1126C>T
ENST00000371113.9:c.1009C>T MANE Select	ENSP00000360154.4:p.Arg337Cys
ENST00000646010.1:c.1057C>T
ENST00000646914.1:c.120C>T
ENST00000647245.1:c.660C>T
ENST00000357121.5:c.1009C>T	ENSP00000349635.5:p.Arg337Cys
ENST00000371113.8:c.1009C>T	ENSP00000360154.4:p.Arg337Cys
NM_000276.3:c.1009C>T	NP_000267.2:p.Arg337Cys
NM_001587.3:c.1009C>T	NP_001578.2:p.Arg337Cys
XM_005262422.1:c.538C>T	XP_005262479.1:p.Arg180Cys
XM_011531342.1:c.1012C>T	XP_011529644.1:p.Arg338Cys
XM_011531343.1:c.1012C>T	XP_011529645.1:p.Arg338Cys
XM_011531344.1:c.865C>T	XP_011529646.1:p.Arg289Cys
XM_011531345.1:c.865C>T	XP_011529647.1:p.Arg289Cys
XM_011531346.1:c.1012C>T	XP_011529648.1:p.Arg338Cys
NM_001318784.1:c.1012C>T	NP_001305713.1:p.Arg338Cys
XM_005262422.2:c.538C>T	XP_005262479.1:p.Arg180Cys
XM_011531344.3:c.865C>T	XP_011529646.1:p.Arg289Cys
XM_011531345.3:c.865C>T	XP_011529647.1:p.Arg289Cys
XM_017029554.1:c.1009C>T	XP_016885043.1:p.Arg337Cys
NM_000276.4:c.1009C>T MANE Select	NP_000267.2:p.Arg337Cys
NM_001318784.2:c.1012C>T	NP_001305713.1:p.Arg338Cys
NM_001587.4:c.1009C>T	NP_001578.2:p.Arg337Cys