Canonical Allele Identifier: CA1969701391
Gene: PTPRJ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.48123468_48123470delinsTGA , CM000673.2:g.48123468_48123470delinsTGA GRCh38
NC_000011.9:g.48145020_48145022delinsTGA , CM000673.1:g.48145020_48145022delinsTGA GRCh37
NC_000011.8:g.48101596_48101598delinsTGA NCBI36
NG_012209.1:g.147911_147913delinsTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000698881.1:c.959-145_959-143delinsTGA ENSP00000514003.1:n.959-145_959-143delinsTGA
ENST00000418331.7:c.617-145_617-143delinsTGA MANE Select ENSP00000400010.2:n.617-145_617-143delinsTGA
ENST00000418331.6:c.617-145_617-143delinsTGA ENSP00000400010.2:n.617-145_617-143delinsTGA
ENST00000440289.6:c.617-145_617-143delinsTGA ENSP00000409733.2:n.617-145_617-143delinsTGA
ENST00000527952.1:c.353-145_353-143delinsTGA ENSP00000435618.1:n.353-145_353-143delinsTGA
ENST00000613246.4:c.617-145_617-143delinsTGA ENSP00000477933.1:n.617-145_617-143delinsTGA
ENST00000615445.4:c.617-145_617-143delinsTGA ENSP00000479342.1:n.617-145_617-143delinsTGA
NM_001098503.1:c.617-145_617-143delinsTGA NP_001091973.1:n.617-145_617-143delinsTGA
NM_002843.3:c.617-145_617-143delinsTGA NP_002834.3:n.617-145_617-143delinsTGA
XM_011520249.1:c.650-145_650-143delinsTGA XP_011518551.1:n.650-145_650-143delinsTGA
XR_930883.1:n.967-145_967-143delinsTGA
XM_017018083.1:c.695-145_695-143delinsTGA XP_016873572.1:n.695-145_695-143delinsTGA
XM_017018084.1:c.638-145_638-143delinsTGA XP_016873573.1:n.638-145_638-143delinsTGA
XM_017018085.1:c.569-145_569-143delinsTGA XP_016873574.1:n.569-145_569-143delinsTGA
XR_930883.2:n.1026-145_1026-143delinsTGA
NM_002843.4:c.617-145_617-143delinsTGA MANE Select NP_002834.3:n.617-145_617-143delinsTGA
NM_001098503.2:c.617-145_617-143delinsTGA NP_001091973.1:n.617-145_617-143delinsTGA