Canonical Allele Identifier: CA1969701468
Gene: PTPRJ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.48123596T= , CM000673.2:g.48123596T= GRCh38
NC_000011.9:g.48145148T= , CM000673.1:g.48145148T= GRCh37
NC_000011.8:g.48101724T= NCBI36
NG_012209.1:g.148039T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698881.1:c.959-17T= ENSP00000514003.1:n.959-17T=
ENST00000418331.7:c.617-17T= MANE Select ENSP00000400010.2:n.617-17T=
ENST00000418331.6:c.617-17T= ENSP00000400010.2:n.617-17T=
ENST00000440289.6:c.617-17T= ENSP00000409733.2:n.617-17T=
ENST00000527952.1:c.353-17T= ENSP00000435618.1:n.353-17T=
ENST00000613246.4:c.617-17T= ENSP00000477933.1:n.617-17T=
ENST00000615445.4:c.617-17T= ENSP00000479342.1:n.617-17T=
NM_001098503.1:c.617-17T= NP_001091973.1:n.617-17T=
NM_002843.3:c.617-17T= NP_002834.3:n.617-17T=
XM_011520249.1:c.650-17T= XP_011518551.1:n.650-17T=
XR_930883.1:n.967-17T=
XM_017018083.1:c.695-17T= XP_016873572.1:n.695-17T=
XM_017018084.1:c.638-17T= XP_016873573.1:n.638-17T=
XM_017018085.1:c.569-17T= XP_016873574.1:n.569-17T=
XR_930883.2:n.1026-17T=
NM_002843.4:c.617-17T= MANE Select NP_002834.3:n.617-17T=
NM_001098503.2:c.617-17T= NP_001091973.1:n.617-17T=