Canonical Allele Identifier: CA1969679198
Gene: PTPRJ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.48069751T>A , CM000673.2:g.48069751T>A GRCh38
NC_000011.9:g.48091303T>A , CM000673.1:g.48091303T>A GRCh37
NC_000011.8:g.48047879T>A NCBI36
NG_012209.1:g.94194T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698881.1:c.439-40307T>A ENSP00000514003.1:n.439-40307T>A
ENST00000418331.7:c.97-40307T>A MANE Select ENSP00000400010.2:n.97-40307T>A
ENST00000418331.6:c.97-40307T>A ENSP00000400010.2:n.97-40307T>A
ENST00000440289.6:c.97-40307T>A ENSP00000409733.2:n.97-40307T>A
ENST00000526550.1:n.170+23420T>A
ENST00000527952.1:c.97-40307T>A ENSP00000435618.1:n.97-40307T>A
ENST00000534219.5:c.97-40307T>A ENSP00000432686.1:n.97-40307T>A
ENST00000613246.4:c.97-40307T>A ENSP00000477933.1:n.97-40307T>A
ENST00000615445.4:c.97-40307T>A ENSP00000479342.1:n.97-40307T>A
NM_001098503.1:c.97-40307T>A NP_001091973.1:n.97-40307T>A
NM_002843.3:c.97-40307T>A NP_002834.3:n.97-40307T>A
XR_930883.1:n.447-40307T>A
XM_017018083.1:c.439-40307T>A XP_016873572.1:n.439-40307T>A
XM_017018084.1:c.118-40307T>A XP_016873573.1:n.118-40307T>A
XM_017018085.1:c.49-40307T>A XP_016873574.1:n.49-40307T>A
XR_930883.2:n.506-40307T>A
NM_002843.4:c.97-40307T>A MANE Select NP_002834.3:n.97-40307T>A
NM_001098503.2:c.97-40307T>A NP_001091973.1:n.97-40307T>A