Canonical Allele Identifier: CA1969701837

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123835C= , CM000673.2:g.48123835C=	GRCh38
NC_000011.9:g.48145387C= , CM000673.1:g.48145387C=	GRCh37
NC_000011.8:g.48101963C=	NCBI36
NG_012209.1:g.148278C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1181C=	ENSP00000514003.1:p.Thr394=
ENST00000418331.7:c.839C= MANE Select	ENSP00000400010.2:p.Thr280=
ENST00000418331.6:c.839C=	ENSP00000400010.2:p.Thr280=
ENST00000440289.6:c.839C=	ENSP00000409733.2:p.Thr280=
ENST00000613246.4:c.839C=	ENSP00000477933.1:p.Thr280=
ENST00000615445.4:c.839C=	ENSP00000479342.1:p.Thr280=
NM_001098503.1:c.839C=	NP_001091973.1:p.Thr280=
NM_002843.3:c.839C=	NP_002834.3:p.Thr280=
XM_011520249.1:c.872C=	XP_011518551.1:p.Thr291=
XR_930883.1:n.1189C=
XM_017018083.1:c.917C=	XP_016873572.1:p.Thr306=
XM_017018084.1:c.860C=	XP_016873573.1:p.Thr287=
XM_017018085.1:c.791C=	XP_016873574.1:p.Thr264=
XR_930883.2:n.1248C=
NM_002843.4:c.839C= MANE Select	NP_002834.3:p.Thr280=
NM_001098503.2:c.839C=	NP_001091973.1:p.Thr280=