Canonical Allele Identifier: CA1969701475

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123614G= , CM000673.2:g.48123614G=	GRCh38
NC_000011.9:g.48145166G= , CM000673.1:g.48145166G=	GRCh37
NC_000011.8:g.48101742G=	NCBI36
NG_012209.1:g.148057G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.960G=	ENSP00000514003.1:p.Glu320=
ENST00000418331.7:c.618G= MANE Select	ENSP00000400010.2:p.Glu206=
ENST00000418331.6:c.618G=	ENSP00000400010.2:p.Glu206=
ENST00000440289.6:c.618G=	ENSP00000409733.2:p.Glu206=
ENST00000527952.1:c.354G=	ENSP00000435618.1:p.Glu118=
ENST00000613246.4:c.618G=	ENSP00000477933.1:p.Glu206=
ENST00000615445.4:c.618G=	ENSP00000479342.1:p.Glu206=
NM_001098503.1:c.618G=	NP_001091973.1:p.Glu206=
NM_002843.3:c.618G=	NP_002834.3:p.Glu206=
XM_011520249.1:c.651G=	XP_011518551.1:p.Glu217=
XR_930883.1:n.968G=
XM_017018083.1:c.696G=	XP_016873572.1:p.Glu232=
XM_017018084.1:c.639G=	XP_016873573.1:p.Glu213=
XM_017018085.1:c.570G=	XP_016873574.1:p.Glu190=
XR_930883.2:n.1027G=
NM_002843.4:c.618G= MANE Select	NP_002834.3:p.Glu206=
NM_001098503.2:c.618G=	NP_001091973.1:p.Glu206=