Canonical Allele Identifier: CA403502168

Gene: PTPRS

Linked Data

• MyVariant Identifiers: chr19:g.5210775T>A (hg19) ; chr19:g.5210764T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5210764T>A , CM000681.2:g.5210764T>A	GRCh38
NC_000019.9:g.5210775T>A , CM000681.1:g.5210775T>A	GRCh37
NC_000019.8:g.5161775T>A	NCBI36
NG_033964.1:g.135040A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706768.1:n.586A>T
ENST00000706769.1:n.411A>T
ENST00000262963.11:c.5276A>T MANE Select	ENSP00000262963.8:p.Glu1759Val
ENST00000262963.10:c.3935A>T	ENSP00000262963.7:p.Glu1312Val
ENST00000348075.6:c.5162A>T	ENSP00000269907.3:p.Glu1721Val
ENST00000353284.6:c.3947A>T	ENSP00000327313.3:p.Glu1316Val
ENST00000357368.8:c.5276A>T	ENSP00000349932.4:p.Glu1759Val
ENST00000587303.5:c.5276A>T	ENSP00000467537.1:p.Glu1759Val
ENST00000588012.5:c.5162A>T	ENSP00000465443.1:p.Glu1721Val
ENST00000588552.5:n.4217A>T
ENST00000592099.5:c.3935A>T	ENSP00000467398.1:p.Glu1312Val
NM_002850.3:c.5276A>T	NP_002841.3:p.Glu1759Val
NM_130853.2:c.3935A>T	NP_570923.2:p.Glu1312Val
NM_130854.2:c.5162A>T	NP_570924.2:p.Glu1721Val
NM_130855.2:c.3947A>T	NP_570925.2:p.Glu1316Val
XM_005259600.1:c.5237A>T	XP_005259657.1:p.Glu1746Val
XM_005259601.2:c.5237A>T	XP_005259658.1:p.Glu1746Val
XM_005259606.1:c.5162A>T	XP_005259663.1:p.Glu1721Val
XM_005259607.1:c.5150A>T	XP_005259664.1:p.Glu1717Val
XM_005259609.1:c.3935A>T	XP_005259666.1:p.Glu1312Val
XM_005259610.1:c.3923A>T	XP_005259667.1:p.Glu1308Val
XM_006722808.1:c.5264A>T	XP_006722871.1:p.Glu1755Val
XM_006722809.2:c.5264A>T	XP_006722872.1:p.Glu1755Val
XM_006722810.2:c.5264A>T	XP_006722873.1:p.Glu1755Val
XM_006722811.1:c.5252A>T	XP_006722874.1:p.Glu1751Val
XM_006722812.1:c.5237A>T	XP_006722875.1:p.Glu1746Val
XM_006722814.1:c.5216A>T	XP_006722877.1:p.Glu1739Val
XM_006722815.1:c.5204A>T	XP_006722878.1:p.Glu1735Val
XM_006722817.1:c.5177A>T	XP_006722880.1:p.Glu1726Val
XM_006722818.1:c.4010A>T	XP_006722881.1:p.Glu1337Val
XM_006722819.1:c.3998A>T	XP_006722882.1:p.Glu1333Val
XM_006722820.1:c.3962A>T	XP_006722883.1:p.Glu1321Val
XM_011528157.1:c.3983A>T	XP_011526459.1:p.Glu1328Val
XM_011528158.1:c.2903A>T	XP_011526460.1:p.Glu968Val
XM_005259600.2:c.5237A>T	XP_005259657.1:p.Glu1746Val
XM_005259606.2:c.5162A>T	XP_005259663.1:p.Glu1721Val
XM_005259607.2:c.5150A>T	XP_005259664.1:p.Glu1717Val
XM_011528157.2:c.3983A>T	XP_011526459.1:p.Glu1328Val
XM_011528158.2:c.2903A>T	XP_011526460.1:p.Glu968Val
XM_017027065.1:c.5249A>T	XP_016882554.1:p.Glu1750Val
XM_017027066.1:c.5249A>T	XP_016882555.1:p.Glu1750Val
XM_017027067.1:c.5249A>T	XP_016882556.1:p.Glu1750Val
XM_017027068.1:c.5237A>T	XP_016882557.1:p.Glu1746Val
XM_017027069.1:c.5222A>T	XP_016882558.1:p.Glu1741Val
XM_017027070.1:c.5201A>T	XP_016882559.1:p.Glu1734Val
XM_017027071.1:c.5189A>T	XP_016882560.1:p.Glu1730Val
XM_017027072.1:c.5162A>T	XP_016882561.1:p.Glu1721Val
XM_017027073.1:c.4523A>T	XP_016882562.1:p.Glu1508Val
XM_017027074.1:c.3995A>T	XP_016882563.1:p.Glu1332Val
XM_017027075.1:c.3983A>T	XP_016882564.1:p.Glu1328Val
XM_017027076.1:c.3947A>T	XP_016882565.1:p.Glu1316Val
NM_002850.4:c.5276A>T MANE Select	NP_002841.3:p.Glu1759Val
NM_130853.3:c.3935A>T	NP_570923.2:p.Glu1312Val
NM_130854.3:c.5162A>T	NP_570924.2:p.Glu1721Val
NM_130855.3:c.3947A>T	NP_570925.2:p.Glu1316Val
NM_001394011.1:c.5210A>T	NP_001380940.1:p.Glu1737Val
NM_001394012.1:c.5189A>T	NP_001380941.1:p.Glu1730Val
NM_001394013.1:c.5150A>T	NP_001380942.1:p.Glu1717Val