Canonical Allele Identifier: CA883329690

Gene: PTPRS

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5209630C>T , CM000681.2:g.5209630C>T	GRCh38
NC_000019.9:g.5209641C>T , CM000681.1:g.5209641C>T	GRCh37
NC_000019.8:g.5160641C>T	NCBI36
NG_033964.1:g.136174G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706768.1:n.797+839G>A
ENST00000706769.1:n.622+839G>A
ENST00000262963.11:c.5487+839G>A MANE Select	ENSP00000262963.8:n.5487+839G>A
ENST00000262963.10:c.4146+839G>A	ENSP00000262963.7:n.4146+839G>A
ENST00000348075.6:c.5373+839G>A	ENSP00000269907.3:n.5373+839G>A
ENST00000353284.6:c.4158+839G>A	ENSP00000327313.3:n.4158+839G>A
ENST00000357368.8:c.5487+839G>A	ENSP00000349932.4:n.5487+839G>A
ENST00000587303.5:c.5487+839G>A	ENSP00000467537.1:n.5487+839G>A
ENST00000588012.5:c.5373+839G>A	ENSP00000465443.1:n.5373+839G>A
ENST00000588552.5:n.4428+839G>A
ENST00000592099.5:c.4146+839G>A	ENSP00000467398.1:n.4146+839G>A
NM_002850.3:c.5487+839G>A	NP_002841.3:n.5487+839G>A
NM_130853.2:c.4146+839G>A	NP_570923.2:n.4146+839G>A
NM_130854.2:c.5373+839G>A	NP_570924.2:n.5373+839G>A
NM_130855.2:c.4158+839G>A	NP_570925.2:n.4158+839G>A
XM_005259600.1:c.5448+839G>A	XP_005259657.1:n.5448+839G>A
XM_005259601.2:c.5448+839G>A	XP_005259658.1:n.5448+839G>A
XM_005259606.1:c.5373+839G>A	XP_005259663.1:n.5373+839G>A
XM_005259607.1:c.5361+839G>A	XP_005259664.1:n.5361+839G>A
XM_005259609.1:c.4146+839G>A	XP_005259666.1:n.4146+839G>A
XM_005259610.1:c.4134+839G>A	XP_005259667.1:n.4134+839G>A
XM_006722808.1:c.5475+839G>A	XP_006722871.1:n.5475+839G>A
XM_006722809.2:c.5475+839G>A	XP_006722872.1:n.5475+839G>A
XM_006722810.2:c.5475+839G>A	XP_006722873.1:n.5475+839G>A
XM_006722811.1:c.5463+839G>A	XP_006722874.1:n.5463+839G>A
XM_006722812.1:c.5448+839G>A	XP_006722875.1:n.5448+839G>A
XM_006722814.1:c.5427+839G>A	XP_006722877.1:n.5427+839G>A
XM_006722815.1:c.5415+839G>A	XP_006722878.1:n.5415+839G>A
XM_006722817.1:c.5388+839G>A	XP_006722880.1:n.5388+839G>A
XM_006722818.1:c.4221+839G>A	XP_006722881.1:n.4221+839G>A
XM_006722819.1:c.4209+839G>A	XP_006722882.1:n.4209+839G>A
XM_006722820.1:c.4173+839G>A	XP_006722883.1:n.4173+839G>A
XM_011528157.1:c.4194+839G>A	XP_011526459.1:n.4194+839G>A
XM_011528158.1:c.3114+839G>A	XP_011526460.1:n.3114+839G>A
XM_005259600.2:c.5448+839G>A	XP_005259657.1:n.5448+839G>A
XM_005259606.2:c.5373+839G>A	XP_005259663.1:n.5373+839G>A
XM_005259607.2:c.5361+839G>A	XP_005259664.1:n.5361+839G>A
XM_011528157.2:c.4194+839G>A	XP_011526459.1:n.4194+839G>A
XM_011528158.2:c.3114+839G>A	XP_011526460.1:n.3114+839G>A
XM_017027065.1:c.5460+839G>A	XP_016882554.1:n.5460+839G>A
XM_017027066.1:c.5460+839G>A	XP_016882555.1:n.5460+839G>A
XM_017027067.1:c.5460+839G>A	XP_016882556.1:n.5460+839G>A
XM_017027068.1:c.5448+839G>A	XP_016882557.1:n.5448+839G>A
XM_017027069.1:c.5433+839G>A	XP_016882558.1:n.5433+839G>A
XM_017027070.1:c.5412+839G>A	XP_016882559.1:n.5412+839G>A
XM_017027071.1:c.5400+839G>A	XP_016882560.1:n.5400+839G>A
XM_017027072.1:c.5373+839G>A	XP_016882561.1:n.5373+839G>A
XM_017027073.1:c.4734+839G>A	XP_016882562.1:n.4734+839G>A
XM_017027074.1:c.4206+839G>A	XP_016882563.1:n.4206+839G>A
XM_017027075.1:c.4194+839G>A	XP_016882564.1:n.4194+839G>A
XM_017027076.1:c.4158+839G>A	XP_016882565.1:n.4158+839G>A
NM_002850.4:c.5487+839G>A MANE Select	NP_002841.3:n.5487+839G>A
NM_130853.3:c.4146+839G>A	NP_570923.2:n.4146+839G>A
NM_130854.3:c.5373+839G>A	NP_570924.2:n.5373+839G>A
NM_130855.3:c.4158+839G>A	NP_570925.2:n.4158+839G>A
NM_001394011.1:c.5421+839G>A	NP_001380940.1:n.5421+839G>A
NM_001394012.1:c.5400+839G>A	NP_001380941.1:n.5400+839G>A
NM_001394013.1:c.5361+839G>A	NP_001380942.1:n.5361+839G>A