Canonical Allele Identifier: CA1969701272
Gene: PTPRJ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.48123276_48123278delinsCTA , CM000673.2:g.48123276_48123278delinsCTA GRCh38
NC_000011.9:g.48144828_48144830delinsCTA , CM000673.1:g.48144828_48144830delinsCTA GRCh37
NC_000011.8:g.48101404_48101406delinsCTA NCBI36
NG_012209.1:g.147719_147721delinsCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000698881.1:c.959-337_959-335delinsCTA ENSP00000514003.1:n.959-337_959-335delinsCTA
ENST00000418331.7:c.617-337_617-335delinsCTA MANE Select ENSP00000400010.2:n.617-337_617-335delinsCTA
ENST00000418331.6:c.617-337_617-335delinsCTA ENSP00000400010.2:n.617-337_617-335delinsCTA
ENST00000440289.6:c.617-337_617-335delinsCTA ENSP00000409733.2:n.617-337_617-335delinsCTA
ENST00000527952.1:c.353-337_353-335delinsCTA ENSP00000435618.1:n.353-337_353-335delinsCTA
ENST00000613246.4:c.617-337_617-335delinsCTA ENSP00000477933.1:n.617-337_617-335delinsCTA
ENST00000615445.4:c.617-337_617-335delinsCTA ENSP00000479342.1:n.617-337_617-335delinsCTA
NM_001098503.1:c.617-337_617-335delinsCTA NP_001091973.1:n.617-337_617-335delinsCTA
NM_002843.3:c.617-337_617-335delinsCTA NP_002834.3:n.617-337_617-335delinsCTA
XM_011520249.1:c.650-337_650-335delinsCTA XP_011518551.1:n.650-337_650-335delinsCTA
XR_930883.1:n.967-337_967-335delinsCTA
XM_017018083.1:c.695-337_695-335delinsCTA XP_016873572.1:n.695-337_695-335delinsCTA
XM_017018084.1:c.638-337_638-335delinsCTA XP_016873573.1:n.638-337_638-335delinsCTA
XM_017018085.1:c.569-337_569-335delinsCTA XP_016873574.1:n.569-337_569-335delinsCTA
XR_930883.2:n.1026-337_1026-335delinsCTA
NM_002843.4:c.617-337_617-335delinsCTA MANE Select NP_002834.3:n.617-337_617-335delinsCTA
NM_001098503.2:c.617-337_617-335delinsCTA NP_001091973.1:n.617-337_617-335delinsCTA