Canonical Allele Identifier: CA1969701547

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123668T= , CM000673.2:g.48123668T=	GRCh38
NC_000011.9:g.48145220T= , CM000673.1:g.48145220T=	GRCh37
NC_000011.8:g.48101796T=	NCBI36
NG_012209.1:g.148111T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1014T=	ENSP00000514003.1:p.Ala338=
ENST00000418331.7:c.672T= MANE Select	ENSP00000400010.2:p.Ala224=
ENST00000418331.6:c.672T=	ENSP00000400010.2:p.Ala224=
ENST00000440289.6:c.672T=	ENSP00000409733.2:p.Ala224=
ENST00000527952.1:c.408T=	ENSP00000435618.1:p.Ala136=
ENST00000613246.4:c.672T=	ENSP00000477933.1:p.Ala224=
ENST00000615445.4:c.672T=	ENSP00000479342.1:p.Ala224=
NM_001098503.1:c.672T=	NP_001091973.1:p.Ala224=
NM_002843.3:c.672T=	NP_002834.3:p.Ala224=
XM_011520249.1:c.705T=	XP_011518551.1:p.Ala235=
XR_930883.1:n.1022T=
XM_017018083.1:c.750T=	XP_016873572.1:p.Ala250=
XM_017018084.1:c.693T=	XP_016873573.1:p.Ala231=
XM_017018085.1:c.624T=	XP_016873574.1:p.Ala208=
XR_930883.2:n.1081T=
NM_002843.4:c.672T= MANE Select	NP_002834.3:p.Ala224=
NM_001098503.2:c.672T=	NP_001091973.1:p.Ala224=