Canonical Allele Identifier: CA1969711413
Community Standard Title: NM_002843.4(PTPRJ):c.2616G= (p.Glu872=)
Gene: PTPRJ HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_002843.4:c.2616G= MANE Select NP_002834.3:p.Glu872=
ENST00000418331.7:c.2616G= MANE Select ENSP00000400010.2:p.Glu872=
NM_002843.3:c.2616G= NP_002834.3:p.Glu872=
ENST00000418331.6:c.2616G= ENSP00000400010.2:p.Glu872=
ENST00000613246.4:c.2616G= ENSP00000477933.1:p.Glu872=
ENST00000615445.4:c.2616G= ENSP00000479342.1:p.Glu872=
ENST00000698881.1:c.2958G= ENSP00000514003.1:p.Glu986=
XM_011520249.1:c.2649G= XP_011518551.1:p.Glu883=
XM_017018083.1:c.2694G= XP_016873572.1:p.Glu898=
XM_017018084.1:c.2637G= XP_016873573.1:p.Glu879=
XM_017018085.1:c.2568G= XP_016873574.1:p.Glu856=
XR_930883.1:n.2966G=
XR_930883.2:n.3025G=