Canonical Allele Identifier: CA1969701832

Gene: PTPRJ

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123833G= , CM000673.2:g.48123833G=	GRCh38
NC_000011.9:g.48145385G= , CM000673.1:g.48145385G=	GRCh37
NC_000011.8:g.48101961G=	NCBI36
NG_012209.1:g.148276G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1179G=	ENSP00000514003.1:p.Lys393=
ENST00000418331.7:c.837G= MANE Select	ENSP00000400010.2:p.Lys279=
ENST00000418331.6:c.837G=	ENSP00000400010.2:p.Lys279=
ENST00000440289.6:c.837G=	ENSP00000409733.2:p.Lys279=
ENST00000613246.4:c.837G=	ENSP00000477933.1:p.Lys279=
ENST00000615445.4:c.837G=	ENSP00000479342.1:p.Lys279=
NM_001098503.1:c.837G=	NP_001091973.1:p.Lys279=
NM_002843.3:c.837G=	NP_002834.3:p.Lys279=
XM_011520249.1:c.870G=	XP_011518551.1:p.Lys290=
XR_930883.1:n.1187G=
XM_017018083.1:c.915G=	XP_016873572.1:p.Lys305=
XM_017018084.1:c.858G=	XP_016873573.1:p.Lys286=
XM_017018085.1:c.789G=	XP_016873574.1:p.Lys263=
XR_930883.2:n.1246G=
NM_002843.4:c.837G= MANE Select	NP_002834.3:p.Lys279=
NM_001098503.2:c.837G=	NP_001091973.1:p.Lys279=