Canonical Allele Identifier: CA1969701726

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123769A= , CM000673.2:g.48123769A=	GRCh38
NC_000011.9:g.48145321A= , CM000673.1:g.48145321A=	GRCh37
NC_000011.8:g.48101897A=	NCBI36
NG_012209.1:g.148212A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1115A=	ENSP00000514003.1:p.Asn372=
ENST00000418331.7:c.773A= MANE Select	ENSP00000400010.2:p.Asn258=
ENST00000418331.6:c.773A=	ENSP00000400010.2:p.Asn258=
ENST00000440289.6:c.773A=	ENSP00000409733.2:p.Asn258=
ENST00000613246.4:c.773A=	ENSP00000477933.1:p.Asn258=
ENST00000615445.4:c.773A=	ENSP00000479342.1:p.Asn258=
NM_001098503.1:c.773A=	NP_001091973.1:p.Asn258=
NM_002843.3:c.773A=	NP_002834.3:p.Asn258=
XM_011520249.1:c.806A=	XP_011518551.1:p.Asn269=
XR_930883.1:n.1123A=
XM_017018083.1:c.851A=	XP_016873572.1:p.Asn284=
XM_017018084.1:c.794A=	XP_016873573.1:p.Asn265=
XM_017018085.1:c.725A=	XP_016873574.1:p.Asn242=
XR_930883.2:n.1182A=
NM_002843.4:c.773A= MANE Select	NP_002834.3:p.Asn258=
NM_001098503.2:c.773A=	NP_001091973.1:p.Asn258=