Canonical Allele Identifier: CA5982491

Gene: PTPRJ

Linked Data

• dbSNP Id: rs4752904
• ExAC: 11:48166267 G / C
• gnomAD v2: 11-48166267-G-C
• gnomAD v3: 11-48144715-G-C
• gnomAD v4: 11-48144715-G-C
• MyVariant Identifiers: chr11:g.48166267G>C (hg19) ; chr11:g.48144715G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48144715G>C , CM000673.2:g.48144715G>C	GRCh38
NC_000011.9:g.48166267G>C , CM000673.1:g.48166267G>C	GRCh37
NC_000011.8:g.48122843G>C	NCBI36
NG_012209.1:g.169158G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.2958G>C	ENSP00000514003.1:p.Glu986Asp
ENST00000418331.7:c.2616G>C MANE Select	ENSP00000400010.2:p.Glu872Asp
ENST00000418331.6:c.2616G>C	ENSP00000400010.2:p.Glu872Asp
ENST00000613246.4:c.2616G>C	ENSP00000477933.1:p.Glu872Asp
ENST00000615445.4:c.2616G>C	ENSP00000479342.1:p.Glu872Asp
NM_002843.3:c.2616G>C	NP_002834.3:p.Glu872Asp
XM_011520249.1:c.2649G>C	XP_011518551.1:p.Glu883Asp
XR_930883.1:n.2966G>C
XM_017018083.1:c.2694G>C	XP_016873572.1:p.Glu898Asp
XM_017018084.1:c.2637G>C	XP_016873573.1:p.Glu879Asp
XM_017018085.1:c.2568G>C	XP_016873574.1:p.Glu856Asp
XR_930883.2:n.3025G>C
NM_002843.4:c.2616G>C MANE Select	NP_002834.3:p.Glu872Asp