Canonical Allele Identifier: CA1969701554
Gene: PTPRJ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.48123680C= , CM000673.2:g.48123680C= GRCh38
NC_000011.9:g.48145232C= , CM000673.1:g.48145232C= GRCh37
NC_000011.8:g.48101808C= NCBI36
NG_012209.1:g.148123C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698881.1:c.1026C= ENSP00000514003.1:p.Ser342=
ENST00000418331.7:c.684C= MANE Select ENSP00000400010.2:p.Ser228=
ENST00000418331.6:c.684C= ENSP00000400010.2:p.Ser228=
ENST00000440289.6:c.684C= ENSP00000409733.2:p.Ser228=
ENST00000527952.1:c.420C= ENSP00000435618.1:p.Ser140=
ENST00000613246.4:c.684C= ENSP00000477933.1:p.Ser228=
ENST00000615445.4:c.684C= ENSP00000479342.1:p.Ser228=
NM_001098503.1:c.684C= NP_001091973.1:p.Ser228=
NM_002843.3:c.684C= NP_002834.3:p.Ser228=
XM_011520249.1:c.717C= XP_011518551.1:p.Ser239=
XR_930883.1:n.1034C=
XM_017018083.1:c.762C= XP_016873572.1:p.Ser254=
XM_017018084.1:c.705C= XP_016873573.1:p.Ser235=
XM_017018085.1:c.636C= XP_016873574.1:p.Ser212=
XR_930883.2:n.1093C=
NM_002843.4:c.684C= MANE Select NP_002834.3:p.Ser228=
NM_001098503.2:c.684C= NP_001091973.1:p.Ser228=