Canonical Allele Identifier: CA1969701802

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123823A= , CM000673.2:g.48123823A=	GRCh38
NC_000011.9:g.48145375A= , CM000673.1:g.48145375A=	GRCh37
NC_000011.8:g.48101951A=	NCBI36
NG_012209.1:g.148266A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1169A=	ENSP00000514003.1:p.Gln390=
ENST00000418331.7:c.827A= MANE Select	ENSP00000400010.2:p.Gln276=
ENST00000418331.6:c.827A=	ENSP00000400010.2:p.Gln276=
ENST00000440289.6:c.827A=	ENSP00000409733.2:p.Gln276=
ENST00000613246.4:c.827A=	ENSP00000477933.1:p.Gln276=
ENST00000615445.4:c.827A=	ENSP00000479342.1:p.Gln276=
NM_001098503.1:c.827A=	NP_001091973.1:p.Gln276=
NM_002843.3:c.827A=	NP_002834.3:p.Gln276=
XM_011520249.1:c.860A=	XP_011518551.1:p.Gln287=
XR_930883.1:n.1177A=
XM_017018083.1:c.905A=	XP_016873572.1:p.Gln302=
XM_017018084.1:c.848A=	XP_016873573.1:p.Gln283=
XM_017018085.1:c.779A=	XP_016873574.1:p.Gln260=
XR_930883.2:n.1236A=
NM_002843.4:c.827A= MANE Select	NP_002834.3:p.Gln276=
NM_001098503.2:c.827A=	NP_001091973.1:p.Gln276=