Canonical Allele Identifier: CA1969701810

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123824A= , CM000673.2:g.48123824A=	GRCh38
NC_000011.9:g.48145376A= , CM000673.1:g.48145376A=	GRCh37
NC_000011.8:g.48101952A=	NCBI36
NG_012209.1:g.148267A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1170A=	ENSP00000514003.1:p.Gln390=
ENST00000418331.7:c.828A= MANE Select	ENSP00000400010.2:p.Gln276=
ENST00000418331.6:c.828A=	ENSP00000400010.2:p.Gln276=
ENST00000440289.6:c.828A=	ENSP00000409733.2:p.Gln276=
ENST00000613246.4:c.828A=	ENSP00000477933.1:p.Gln276=
ENST00000615445.4:c.828A=	ENSP00000479342.1:p.Gln276=
NM_001098503.1:c.828A=	NP_001091973.1:p.Gln276=
NM_002843.3:c.828A=	NP_002834.3:p.Gln276=
XM_011520249.1:c.861A=	XP_011518551.1:p.Gln287=
XR_930883.1:n.1178A=
XM_017018083.1:c.906A=	XP_016873572.1:p.Gln302=
XM_017018084.1:c.849A=	XP_016873573.1:p.Gln283=
XM_017018085.1:c.780A=	XP_016873574.1:p.Gln260=
XR_930883.2:n.1237A=
NM_002843.4:c.828A= MANE Select	NP_002834.3:p.Gln276=
NM_001098503.2:c.828A=	NP_001091973.1:p.Gln276=