Canonical Allele Identifier: CA403502162

Gene: PTPRS

Linked Data

• MyVariant Identifiers: chr19:g.5210772G>C (hg19) ; chr19:g.5210761G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5210761G>C , CM000681.2:g.5210761G>C	GRCh38
NC_000019.9:g.5210772G>C , CM000681.1:g.5210772G>C	GRCh37
NC_000019.8:g.5161772G>C	NCBI36
NG_033964.1:g.135043C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706768.1:n.589C>G
ENST00000706769.1:n.414C>G
ENST00000262963.11:c.5279C>G MANE Select	ENSP00000262963.8:p.Thr1760Ser
ENST00000262963.10:c.3938C>G	ENSP00000262963.7:p.Thr1313Ser
ENST00000348075.6:c.5165C>G	ENSP00000269907.3:p.Thr1722Ser
ENST00000353284.6:c.3950C>G	ENSP00000327313.3:p.Thr1317Ser
ENST00000357368.8:c.5279C>G	ENSP00000349932.4:p.Thr1760Ser
ENST00000587303.5:c.5279C>G	ENSP00000467537.1:p.Thr1760Ser
ENST00000588012.5:c.5165C>G	ENSP00000465443.1:p.Thr1722Ser
ENST00000588552.5:n.4220C>G
ENST00000592099.5:c.3938C>G	ENSP00000467398.1:p.Thr1313Ser
NM_002850.3:c.5279C>G	NP_002841.3:p.Thr1760Ser
NM_130853.2:c.3938C>G	NP_570923.2:p.Thr1313Ser
NM_130854.2:c.5165C>G	NP_570924.2:p.Thr1722Ser
NM_130855.2:c.3950C>G	NP_570925.2:p.Thr1317Ser
XM_005259600.1:c.5240C>G	XP_005259657.1:p.Thr1747Ser
XM_005259601.2:c.5240C>G	XP_005259658.1:p.Thr1747Ser
XM_005259606.1:c.5165C>G	XP_005259663.1:p.Thr1722Ser
XM_005259607.1:c.5153C>G	XP_005259664.1:p.Thr1718Ser
XM_005259609.1:c.3938C>G	XP_005259666.1:p.Thr1313Ser
XM_005259610.1:c.3926C>G	XP_005259667.1:p.Thr1309Ser
XM_006722808.1:c.5267C>G	XP_006722871.1:p.Thr1756Ser
XM_006722809.2:c.5267C>G	XP_006722872.1:p.Thr1756Ser
XM_006722810.2:c.5267C>G	XP_006722873.1:p.Thr1756Ser
XM_006722811.1:c.5255C>G	XP_006722874.1:p.Thr1752Ser
XM_006722812.1:c.5240C>G	XP_006722875.1:p.Thr1747Ser
XM_006722814.1:c.5219C>G	XP_006722877.1:p.Thr1740Ser
XM_006722815.1:c.5207C>G	XP_006722878.1:p.Thr1736Ser
XM_006722817.1:c.5180C>G	XP_006722880.1:p.Thr1727Ser
XM_006722818.1:c.4013C>G	XP_006722881.1:p.Thr1338Ser
XM_006722819.1:c.4001C>G	XP_006722882.1:p.Thr1334Ser
XM_006722820.1:c.3965C>G	XP_006722883.1:p.Thr1322Ser
XM_011528157.1:c.3986C>G	XP_011526459.1:p.Thr1329Ser
XM_011528158.1:c.2906C>G	XP_011526460.1:p.Thr969Ser
XM_005259600.2:c.5240C>G	XP_005259657.1:p.Thr1747Ser
XM_005259606.2:c.5165C>G	XP_005259663.1:p.Thr1722Ser
XM_005259607.2:c.5153C>G	XP_005259664.1:p.Thr1718Ser
XM_011528157.2:c.3986C>G	XP_011526459.1:p.Thr1329Ser
XM_011528158.2:c.2906C>G	XP_011526460.1:p.Thr969Ser
XM_017027065.1:c.5252C>G	XP_016882554.1:p.Thr1751Ser
XM_017027066.1:c.5252C>G	XP_016882555.1:p.Thr1751Ser
XM_017027067.1:c.5252C>G	XP_016882556.1:p.Thr1751Ser
XM_017027068.1:c.5240C>G	XP_016882557.1:p.Thr1747Ser
XM_017027069.1:c.5225C>G	XP_016882558.1:p.Thr1742Ser
XM_017027070.1:c.5204C>G	XP_016882559.1:p.Thr1735Ser
XM_017027071.1:c.5192C>G	XP_016882560.1:p.Thr1731Ser
XM_017027072.1:c.5165C>G	XP_016882561.1:p.Thr1722Ser
XM_017027073.1:c.4526C>G	XP_016882562.1:p.Thr1509Ser
XM_017027074.1:c.3998C>G	XP_016882563.1:p.Thr1333Ser
XM_017027075.1:c.3986C>G	XP_016882564.1:p.Thr1329Ser
XM_017027076.1:c.3950C>G	XP_016882565.1:p.Thr1317Ser
NM_002850.4:c.5279C>G MANE Select	NP_002841.3:p.Thr1760Ser
NM_130853.3:c.3938C>G	NP_570923.2:p.Thr1313Ser
NM_130854.3:c.5165C>G	NP_570924.2:p.Thr1722Ser
NM_130855.3:c.3950C>G	NP_570925.2:p.Thr1317Ser
NM_001394011.1:c.5213C>G	NP_001380940.1:p.Thr1738Ser
NM_001394012.1:c.5192C>G	NP_001380941.1:p.Thr1731Ser
NM_001394013.1:c.5153C>G	NP_001380942.1:p.Thr1718Ser