Canonical Allele Identifier: CA505177070

Gene: PTPRS

Linked Data

• dbSNP Id: rs201047108
• MyVariant Identifiers: chr19:g.5210768C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5210757C>A , CM000681.2:g.5210757C>A	GRCh38
NC_000019.9:g.5210768C>A , CM000681.1:g.5210768C>A	GRCh37
NC_000019.8:g.5161768C>A	NCBI36
NG_033964.1:g.135047G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706768.1:n.593G>T
ENST00000706769.1:n.418G>T
ENST00000262963.11:c.5283G>T MANE Select	ENSP00000262963.8:p.Thr1761=
ENST00000262963.10:c.3942G>T	ENSP00000262963.7:p.Thr1314=
ENST00000348075.6:c.5169G>T	ENSP00000269907.3:p.Thr1723=
ENST00000353284.6:c.3954G>T	ENSP00000327313.3:p.Thr1318=
ENST00000357368.8:c.5283G>T	ENSP00000349932.4:p.Thr1761=
ENST00000587303.5:c.5283G>T	ENSP00000467537.1:p.Thr1761=
ENST00000588012.5:c.5169G>T	ENSP00000465443.1:p.Thr1723=
ENST00000588552.5:n.4224G>T
ENST00000592099.5:c.3942G>T	ENSP00000467398.1:p.Thr1314=
NM_002850.3:c.5283G>T	NP_002841.3:p.Thr1761=
NM_130853.2:c.3942G>T	NP_570923.2:p.Thr1314=
NM_130854.2:c.5169G>T	NP_570924.2:p.Thr1723=
NM_130855.2:c.3954G>T	NP_570925.2:p.Thr1318=
XM_005259600.1:c.5244G>T	XP_005259657.1:p.Thr1748=
XM_005259601.2:c.5244G>T	XP_005259658.1:p.Thr1748=
XM_005259606.1:c.5169G>T	XP_005259663.1:p.Thr1723=
XM_005259607.1:c.5157G>T	XP_005259664.1:p.Thr1719=
XM_005259609.1:c.3942G>T	XP_005259666.1:p.Thr1314=
XM_005259610.1:c.3930G>T	XP_005259667.1:p.Thr1310=
XM_006722808.1:c.5271G>T	XP_006722871.1:p.Thr1757=
XM_006722809.2:c.5271G>T	XP_006722872.1:p.Thr1757=
XM_006722810.2:c.5271G>T	XP_006722873.1:p.Thr1757=
XM_006722811.1:c.5259G>T	XP_006722874.1:p.Thr1753=
XM_006722812.1:c.5244G>T	XP_006722875.1:p.Thr1748=
XM_006722814.1:c.5223G>T	XP_006722877.1:p.Thr1741=
XM_006722815.1:c.5211G>T	XP_006722878.1:p.Thr1737=
XM_006722817.1:c.5184G>T	XP_006722880.1:p.Thr1728=
XM_006722818.1:c.4017G>T	XP_006722881.1:p.Thr1339=
XM_006722819.1:c.4005G>T	XP_006722882.1:p.Thr1335=
XM_006722820.1:c.3969G>T	XP_006722883.1:p.Thr1323=
XM_011528157.1:c.3990G>T	XP_011526459.1:p.Thr1330=
XM_011528158.1:c.2910G>T	XP_011526460.1:p.Thr970=
XM_005259600.2:c.5244G>T	XP_005259657.1:p.Thr1748=
XM_005259606.2:c.5169G>T	XP_005259663.1:p.Thr1723=
XM_005259607.2:c.5157G>T	XP_005259664.1:p.Thr1719=
XM_011528157.2:c.3990G>T	XP_011526459.1:p.Thr1330=
XM_011528158.2:c.2910G>T	XP_011526460.1:p.Thr970=
XM_017027065.1:c.5256G>T	XP_016882554.1:p.Thr1752=
XM_017027066.1:c.5256G>T	XP_016882555.1:p.Thr1752=
XM_017027067.1:c.5256G>T	XP_016882556.1:p.Thr1752=
XM_017027068.1:c.5244G>T	XP_016882557.1:p.Thr1748=
XM_017027069.1:c.5229G>T	XP_016882558.1:p.Thr1743=
XM_017027070.1:c.5208G>T	XP_016882559.1:p.Thr1736=
XM_017027071.1:c.5196G>T	XP_016882560.1:p.Thr1732=
XM_017027072.1:c.5169G>T	XP_016882561.1:p.Thr1723=
XM_017027073.1:c.4530G>T	XP_016882562.1:p.Thr1510=
XM_017027074.1:c.4002G>T	XP_016882563.1:p.Thr1334=
XM_017027075.1:c.3990G>T	XP_016882564.1:p.Thr1330=
XM_017027076.1:c.3954G>T	XP_016882565.1:p.Thr1318=
NM_002850.4:c.5283G>T MANE Select	NP_002841.3:p.Thr1761=
NM_130853.3:c.3942G>T	NP_570923.2:p.Thr1314=
NM_130854.3:c.5169G>T	NP_570924.2:p.Thr1723=
NM_130855.3:c.3954G>T	NP_570925.2:p.Thr1318=
NM_001394011.1:c.5217G>T	NP_001380940.1:p.Thr1739=
NM_001394012.1:c.5196G>T	NP_001380941.1:p.Thr1732=
NM_001394013.1:c.5157G>T	NP_001380942.1:p.Thr1719=