Canonical Allele Identifier: CA1969702959

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48125070G= , CM000673.2:g.48125070G=	GRCh38
NC_000011.9:g.48146622G= , CM000673.1:g.48146622G=	GRCh37
NC_000011.8:g.48103198G=	NCBI36
NG_012209.1:g.149513G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1319G=	ENSP00000514003.1:p.Arg440=
ENST00000418331.7:c.977G= MANE Select	ENSP00000400010.2:p.Arg326=
ENST00000418331.6:c.977G=	ENSP00000400010.2:p.Arg326=
ENST00000440289.6:c.977G=	ENSP00000409733.2:p.Arg326=
ENST00000613246.4:c.977G=	ENSP00000477933.1:p.Arg326=
ENST00000615445.4:c.977G=	ENSP00000479342.1:p.Arg326=
NM_001098503.1:c.977G=	NP_001091973.1:p.Arg326=
NM_002843.3:c.977G=	NP_002834.3:p.Arg326=
XM_011520249.1:c.1010G=	XP_011518551.1:p.Arg337=
XR_930883.1:n.1327G=
XM_017018083.1:c.1055G=	XP_016873572.1:p.Arg352=
XM_017018084.1:c.998G=	XP_016873573.1:p.Arg333=
XM_017018085.1:c.929G=	XP_016873574.1:p.Arg310=
XR_930883.2:n.1386G=
NM_002843.4:c.977G= MANE Select	NP_002834.3:p.Arg326=
NM_001098503.2:c.977G=	NP_001091973.1:p.Arg326=