Canonical Allele Identifier: CA2574821348

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123858_48123859del , CM000673.2:g.48123858_48123859del	GRCh38
NC_000011.9:g.48145410_48145411del , CM000673.1:g.48145410_48145411del	GRCh37
NC_000011.8:g.48101986_48101987del	NCBI36
NG_012209.1:g.148301_148302del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1204_1205del	ENSP00000514003.1:p.Glu402ArgfsTer22
ENST00000418331.7:c.862_863del MANE Select	ENSP00000400010.2:p.Glu288ArgfsTer22
ENST00000418331.6:c.862_863del	ENSP00000400010.2:p.Glu288ArgfsTer22
ENST00000440289.6:c.862_863del	ENSP00000409733.2:p.Glu288ArgfsTer22
ENST00000613246.4:c.862_863del	ENSP00000477933.1:p.Glu288ArgfsTer22
ENST00000615445.4:c.862_863del	ENSP00000479342.1:p.Glu288ArgfsTer22
NM_001098503.1:c.862_863del	NP_001091973.1:p.Glu288ArgfsTer22
NM_002843.3:c.862_863del	NP_002834.3:p.Glu288ArgfsTer22
XM_011520249.1:c.895_896del	XP_011518551.1:p.Glu299ArgfsTer22
XR_930883.1:n.1212_1213del
XM_017018083.1:c.940_941del	XP_016873572.1:p.Glu314ArgfsTer22
XM_017018084.1:c.883_884del	XP_016873573.1:p.Glu295ArgfsTer22
XM_017018085.1:c.814_815del	XP_016873574.1:p.Glu272ArgfsTer22
XR_930883.2:n.1271_1272del
NM_002843.4:c.862_863del MANE Select	NP_002834.3:p.Glu288ArgfsTer22
NM_001098503.2:c.862_863del	NP_001091973.1:p.Glu288ArgfsTer22