Canonical Allele Identifier: CA1969701856

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123848C= , CM000673.2:g.48123848C=	GRCh38
NC_000011.9:g.48145400C= , CM000673.1:g.48145400C=	GRCh37
NC_000011.8:g.48101976C=	NCBI36
NG_012209.1:g.148291C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1194C=	ENSP00000514003.1:p.Pro398=
ENST00000418331.7:c.852C= MANE Select	ENSP00000400010.2:p.Pro284=
ENST00000418331.6:c.852C=	ENSP00000400010.2:p.Pro284=
ENST00000440289.6:c.852C=	ENSP00000409733.2:p.Pro284=
ENST00000613246.4:c.852C=	ENSP00000477933.1:p.Pro284=
ENST00000615445.4:c.852C=	ENSP00000479342.1:p.Pro284=
NM_001098503.1:c.852C=	NP_001091973.1:p.Pro284=
NM_002843.3:c.852C=	NP_002834.3:p.Pro284=
XM_011520249.1:c.885C=	XP_011518551.1:p.Pro295=
XR_930883.1:n.1202C=
XM_017018083.1:c.930C=	XP_016873572.1:p.Pro310=
XM_017018084.1:c.873C=	XP_016873573.1:p.Pro291=
XM_017018085.1:c.804C=	XP_016873574.1:p.Pro268=
XR_930883.2:n.1261C=
NM_002843.4:c.852C= MANE Select	NP_002834.3:p.Pro284=
NM_001098503.2:c.852C=	NP_001091973.1:p.Pro284=