Canonical Allele Identifier: CA1969701486

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123622C= , CM000673.2:g.48123622C=	GRCh38
NC_000011.9:g.48145174C= , CM000673.1:g.48145174C=	GRCh37
NC_000011.8:g.48101750C=	NCBI36
NG_012209.1:g.148065C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.968C=	ENSP00000514003.1:p.Pro323=
ENST00000418331.7:c.626C= MANE Select	ENSP00000400010.2:p.Pro209=
ENST00000418331.6:c.626C=	ENSP00000400010.2:p.Pro209=
ENST00000440289.6:c.626C=	ENSP00000409733.2:p.Pro209=
ENST00000527952.1:c.362C=	ENSP00000435618.1:p.Pro121=
ENST00000613246.4:c.626C=	ENSP00000477933.1:p.Pro209=
ENST00000615445.4:c.626C=	ENSP00000479342.1:p.Pro209=
NM_001098503.1:c.626C=	NP_001091973.1:p.Pro209=
NM_002843.3:c.626C=	NP_002834.3:p.Pro209=
XM_011520249.1:c.659C=	XP_011518551.1:p.Pro220=
XR_930883.1:n.976C=
XM_017018083.1:c.704C=	XP_016873572.1:p.Pro235=
XM_017018084.1:c.647C=	XP_016873573.1:p.Pro216=
XM_017018085.1:c.578C=	XP_016873574.1:p.Pro193=
XR_930883.2:n.1035C=
NM_002843.4:c.626C= MANE Select	NP_002834.3:p.Pro209=
NM_001098503.2:c.626C=	NP_001091973.1:p.Pro209=