Canonical Allele Identifier: CA1969701828

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123830T= , CM000673.2:g.48123830T=	GRCh38
NC_000011.9:g.48145382T= , CM000673.1:g.48145382T=	GRCh37
NC_000011.8:g.48101958T=	NCBI36
NG_012209.1:g.148273T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1176T=	ENSP00000514003.1:p.Asn392=
ENST00000418331.7:c.834T= MANE Select	ENSP00000400010.2:p.Asn278=
ENST00000418331.6:c.834T=	ENSP00000400010.2:p.Asn278=
ENST00000440289.6:c.834T=	ENSP00000409733.2:p.Asn278=
ENST00000613246.4:c.834T=	ENSP00000477933.1:p.Asn278=
ENST00000615445.4:c.834T=	ENSP00000479342.1:p.Asn278=
NM_001098503.1:c.834T=	NP_001091973.1:p.Asn278=
NM_002843.3:c.834T=	NP_002834.3:p.Asn278=
XM_011520249.1:c.867T=	XP_011518551.1:p.Asn289=
XR_930883.1:n.1184T=
XM_017018083.1:c.912T=	XP_016873572.1:p.Asn304=
XM_017018084.1:c.855T=	XP_016873573.1:p.Asn285=
XM_017018085.1:c.786T=	XP_016873574.1:p.Asn262=
XR_930883.2:n.1243T=
NM_002843.4:c.834T= MANE Select	NP_002834.3:p.Asn278=
NM_001098503.2:c.834T=	NP_001091973.1:p.Asn278=