Canonical Allele Identifier: CA14719013

Gene: PTPRS

Linked Data

• dbSNP Id: rs4807015
• gnomAD v2: 19-5231135-T-C
• gnomAD v3: 19-5231124-T-C
• gnomAD v4: 19-5231124-T-C
• MyVariant Identifiers: chr19:g.5231135T>C (hg19) ; chr19:g.5231124T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5231124T>C , CM000681.2:g.5231124T>C	GRCh38
NC_000019.9:g.5231135T>C , CM000681.1:g.5231135T>C	GRCh37
NC_000019.8:g.5182135T>C	NCBI36
NG_033964.1:g.114680A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000262963.11:c.2155+186A>G MANE Select	ENSP00000262963.8:n.2155+186A>G
ENST00000262963.10:c.1810+7795A>G	ENSP00000262963.7:n.1810+7795A>G
ENST00000348075.6:c.2116+186A>G	ENSP00000269907.3:n.2116+186A>G
ENST00000353284.6:c.1822+7795A>G	ENSP00000327313.3:n.1822+7795A>G
ENST00000357368.8:c.2155+186A>G	ENSP00000349932.4:n.2155+186A>G
ENST00000587303.5:c.2155+186A>G	ENSP00000467537.1:n.2155+186A>G
ENST00000588012.5:c.2116+186A>G	ENSP00000465443.1:n.2116+186A>G
ENST00000588552.5:n.2044+7795A>G
ENST00000592099.5:c.1810+7795A>G	ENSP00000467398.1:n.1810+7795A>G
NM_002850.3:c.2155+186A>G	NP_002841.3:n.2155+186A>G
NM_130853.2:c.1810+7795A>G	NP_570923.2:n.1810+7795A>G
NM_130854.2:c.2116+186A>G	NP_570924.2:n.2116+186A>G
NM_130855.2:c.1822+7795A>G	NP_570925.2:n.1822+7795A>G
XM_005259600.1:c.2116+186A>G	XP_005259657.1:n.2116+186A>G
XM_005259601.2:c.2116+186A>G	XP_005259658.1:n.2116+186A>G
XM_005259606.1:c.2116+186A>G	XP_005259663.1:n.2116+186A>G
XM_005259607.1:c.2116+186A>G	XP_005259664.1:n.2116+186A>G
XM_005259609.1:c.1810+7795A>G	XP_005259666.1:n.1810+7795A>G
XM_005259610.1:c.1810+7795A>G	XP_005259667.1:n.1810+7795A>G
XM_006722808.1:c.2143+186A>G	XP_006722871.1:n.2143+186A>G
XM_006722809.2:c.2143+186A>G	XP_006722872.1:n.2143+186A>G
XM_006722810.2:c.2143+186A>G	XP_006722873.1:n.2143+186A>G
XM_006722811.1:c.2143+186A>G	XP_006722874.1:n.2143+186A>G
XM_006722812.1:c.2143+186A>G	XP_006722875.1:n.2143+186A>G
XM_006722814.1:c.2143+186A>G	XP_006722877.1:n.2143+186A>G
XM_006722815.1:c.2143+186A>G	XP_006722878.1:n.2143+186A>G
XM_006722817.1:c.2143+186A>G	XP_006722880.1:n.2143+186A>G
XM_006722818.1:c.1837+7795A>G	XP_006722881.1:n.1837+7795A>G
XM_006722819.1:c.1837+7795A>G	XP_006722882.1:n.1837+7795A>G
XM_006722820.1:c.1837+7795A>G	XP_006722883.1:n.1837+7795A>G
XM_011528157.1:c.1810+7795A>G	XP_011526459.1:n.1810+7795A>G
XM_011528158.1:c.3+186A>G	XP_011526460.1:n.3+186A>G
XM_005259600.2:c.2116+186A>G	XP_005259657.1:n.2116+186A>G
XM_005259606.2:c.2116+186A>G	XP_005259663.1:n.2116+186A>G
XM_005259607.2:c.2116+186A>G	XP_005259664.1:n.2116+186A>G
XM_011528157.2:c.1810+7795A>G	XP_011526459.1:n.1810+7795A>G
XM_011528158.2:c.3+186A>G	XP_011526460.1:n.3+186A>G
XM_017027065.1:c.2128+186A>G	XP_016882554.1:n.2128+186A>G
XM_017027066.1:c.2128+186A>G	XP_016882555.1:n.2128+186A>G
XM_017027067.1:c.2128+186A>G	XP_016882556.1:n.2128+186A>G
XM_017027068.1:c.2128+186A>G	XP_016882557.1:n.2128+186A>G
XM_017027069.1:c.2128+186A>G	XP_016882558.1:n.2128+186A>G
XM_017027070.1:c.2128+186A>G	XP_016882559.1:n.2128+186A>G
XM_017027071.1:c.2128+186A>G	XP_016882560.1:n.2128+186A>G
XM_017027072.1:c.2128+186A>G	XP_016882561.1:n.2128+186A>G
XM_017027073.1:c.1402+186A>G	XP_016882562.1:n.1402+186A>G
XM_017027074.1:c.1822+7795A>G	XP_016882563.1:n.1822+7795A>G
XM_017027075.1:c.1822+7795A>G	XP_016882564.1:n.1822+7795A>G
XM_017027076.1:c.1822+7795A>G	XP_016882565.1:n.1822+7795A>G
NM_002850.4:c.2155+186A>G MANE Select	NP_002841.3:n.2155+186A>G
NM_130853.3:c.1810+7795A>G	NP_570923.2:n.1810+7795A>G
NM_130854.3:c.2116+186A>G	NP_570924.2:n.2116+186A>G
NM_130855.3:c.1822+7795A>G	NP_570925.2:n.1822+7795A>G
NM_001394011.1:c.2116+186A>G	NP_001380940.1:n.2116+186A>G
NM_001394012.1:c.2116+186A>G	NP_001380941.1:n.2116+186A>G
NM_001394013.1:c.2116+186A>G	NP_001380942.1:n.2116+186A>G