Canonical Allele Identifier: CA414616273

Gene: OCRL

Linked Data

• MyVariant Identifiers: chrX:g.128703252G>T (hg19) ; chrX:g.129569275G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.129569275G>T , CM000685.2:g.129569275G>T	GRCh38
NC_000023.10:g.128703252G>T , CM000685.1:g.128703252G>T	GRCh37
NC_000023.9:g.128530933G>T	NCBI36
NG_008638.1:g.34001G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000691455.1:c.*1770G>T	ENSP00000510265.1:n.*1770G>T
ENST00000693473.1:c.1595G>T
ENST00000371113.9:c.1478G>T MANE Select	ENSP00000360154.4:p.Arg493Leu
ENST00000646010.1:c.1526G>T
ENST00000646914.1:c.589G>T
ENST00000647245.1:c.1129G>T
ENST00000357121.5:c.1478G>T	ENSP00000349635.5:p.Arg493Leu
ENST00000371113.8:c.1478G>T	ENSP00000360154.4:p.Arg493Leu
NM_000276.3:c.1478G>T	NP_000267.2:p.Arg493Leu
NM_001587.3:c.1478G>T	NP_001578.2:p.Arg493Leu
XM_005262422.1:c.1007G>T	XP_005262479.1:p.Arg336Leu
XM_011531342.1:c.1481G>T	XP_011529644.1:p.Arg494Leu
XM_011531343.1:c.1481G>T	XP_011529645.1:p.Arg494Leu
XM_011531344.1:c.1334G>T	XP_011529646.1:p.Arg445Leu
XM_011531345.1:c.1334G>T	XP_011529647.1:p.Arg445Leu
XM_011531346.1:c.1481G>T	XP_011529648.1:p.Arg494Leu
NM_001318784.1:c.1481G>T	NP_001305713.1:p.Arg494Leu
XM_005262422.2:c.1007G>T	XP_005262479.1:p.Arg336Leu
XM_011531344.3:c.1334G>T	XP_011529646.1:p.Arg445Leu
XM_011531345.3:c.1334G>T	XP_011529647.1:p.Arg445Leu
XM_017029554.1:c.1478G>T	XP_016885043.1:p.Arg493Leu
NM_000276.4:c.1478G>T MANE Select	NP_000267.2:p.Arg493Leu
NM_001318784.2:c.1481G>T	NP_001305713.1:p.Arg494Leu
NM_001587.4:c.1478G>T	NP_001578.2:p.Arg493Leu