Canonical Allele Identifier: CA9108784

Gene: PTPRS

Linked Data

• dbSNP Id: rs759194375
• ExAC: 19:5210774 C / G
• MyVariant Identifiers: chr19:g.5210774C>G (hg19) ; chr19:g.5210763C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5210763C>G , CM000681.2:g.5210763C>G	GRCh38
NC_000019.9:g.5210774C>G , CM000681.1:g.5210774C>G	GRCh37
NC_000019.8:g.5161774C>G	NCBI36
NG_033964.1:g.135041G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706768.1:n.587G>C
ENST00000706769.1:n.412G>C
ENST00000262963.11:c.5277G>C MANE Select	ENSP00000262963.8:p.Glu1759Asp
ENST00000262963.10:c.3936G>C	ENSP00000262963.7:p.Glu1312Asp
ENST00000348075.6:c.5163G>C	ENSP00000269907.3:p.Glu1721Asp
ENST00000353284.6:c.3948G>C	ENSP00000327313.3:p.Glu1316Asp
ENST00000357368.8:c.5277G>C	ENSP00000349932.4:p.Glu1759Asp
ENST00000587303.5:c.5277G>C	ENSP00000467537.1:p.Glu1759Asp
ENST00000588012.5:c.5163G>C	ENSP00000465443.1:p.Glu1721Asp
ENST00000588552.5:n.4218G>C
ENST00000592099.5:c.3936G>C	ENSP00000467398.1:p.Glu1312Asp
NM_002850.3:c.5277G>C	NP_002841.3:p.Glu1759Asp
NM_130853.2:c.3936G>C	NP_570923.2:p.Glu1312Asp
NM_130854.2:c.5163G>C	NP_570924.2:p.Glu1721Asp
NM_130855.2:c.3948G>C	NP_570925.2:p.Glu1316Asp
XM_005259600.1:c.5238G>C	XP_005259657.1:p.Glu1746Asp
XM_005259601.2:c.5238G>C	XP_005259658.1:p.Glu1746Asp
XM_005259606.1:c.5163G>C	XP_005259663.1:p.Glu1721Asp
XM_005259607.1:c.5151G>C	XP_005259664.1:p.Glu1717Asp
XM_005259609.1:c.3936G>C	XP_005259666.1:p.Glu1312Asp
XM_005259610.1:c.3924G>C	XP_005259667.1:p.Glu1308Asp
XM_006722808.1:c.5265G>C	XP_006722871.1:p.Glu1755Asp
XM_006722809.2:c.5265G>C	XP_006722872.1:p.Glu1755Asp
XM_006722810.2:c.5265G>C	XP_006722873.1:p.Glu1755Asp
XM_006722811.1:c.5253G>C	XP_006722874.1:p.Glu1751Asp
XM_006722812.1:c.5238G>C	XP_006722875.1:p.Glu1746Asp
XM_006722814.1:c.5217G>C	XP_006722877.1:p.Glu1739Asp
XM_006722815.1:c.5205G>C	XP_006722878.1:p.Glu1735Asp
XM_006722817.1:c.5178G>C	XP_006722880.1:p.Glu1726Asp
XM_006722818.1:c.4011G>C	XP_006722881.1:p.Glu1337Asp
XM_006722819.1:c.3999G>C	XP_006722882.1:p.Glu1333Asp
XM_006722820.1:c.3963G>C	XP_006722883.1:p.Glu1321Asp
XM_011528157.1:c.3984G>C	XP_011526459.1:p.Glu1328Asp
XM_011528158.1:c.2904G>C	XP_011526460.1:p.Glu968Asp
XM_005259600.2:c.5238G>C	XP_005259657.1:p.Glu1746Asp
XM_005259606.2:c.5163G>C	XP_005259663.1:p.Glu1721Asp
XM_005259607.2:c.5151G>C	XP_005259664.1:p.Glu1717Asp
XM_011528157.2:c.3984G>C	XP_011526459.1:p.Glu1328Asp
XM_011528158.2:c.2904G>C	XP_011526460.1:p.Glu968Asp
XM_017027065.1:c.5250G>C	XP_016882554.1:p.Glu1750Asp
XM_017027066.1:c.5250G>C	XP_016882555.1:p.Glu1750Asp
XM_017027067.1:c.5250G>C	XP_016882556.1:p.Glu1750Asp
XM_017027068.1:c.5238G>C	XP_016882557.1:p.Glu1746Asp
XM_017027069.1:c.5223G>C	XP_016882558.1:p.Glu1741Asp
XM_017027070.1:c.5202G>C	XP_016882559.1:p.Glu1734Asp
XM_017027071.1:c.5190G>C	XP_016882560.1:p.Glu1730Asp
XM_017027072.1:c.5163G>C	XP_016882561.1:p.Glu1721Asp
XM_017027073.1:c.4524G>C	XP_016882562.1:p.Glu1508Asp
XM_017027074.1:c.3996G>C	XP_016882563.1:p.Glu1332Asp
XM_017027075.1:c.3984G>C	XP_016882564.1:p.Glu1328Asp
XM_017027076.1:c.3948G>C	XP_016882565.1:p.Glu1316Asp
NM_002850.4:c.5277G>C MANE Select	NP_002841.3:p.Glu1759Asp
NM_130853.3:c.3936G>C	NP_570923.2:p.Glu1312Asp
NM_130854.3:c.5163G>C	NP_570924.2:p.Glu1721Asp
NM_130855.3:c.3948G>C	NP_570925.2:p.Glu1316Asp
NM_001394011.1:c.5211G>C	NP_001380940.1:p.Glu1737Asp
NM_001394012.1:c.5190G>C	NP_001380941.1:p.Glu1730Asp
NM_001394013.1:c.5151G>C	NP_001380942.1:p.Glu1717Asp