Canonical Allele Identifier: CA380370754

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145392G>C (hg19) ; chr11:g.48123840G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123840G>C , CM000673.2:g.48123840G>C	GRCh38
NC_000011.9:g.48145392G>C , CM000673.1:g.48145392G>C	GRCh37
NC_000011.8:g.48101968G>C	NCBI36
NG_012209.1:g.148283G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1186G>C	ENSP00000514003.1:p.Gly396Arg
ENST00000418331.7:c.844G>C MANE Select	ENSP00000400010.2:p.Gly282Arg
ENST00000418331.6:c.844G>C	ENSP00000400010.2:p.Gly282Arg
ENST00000440289.6:c.844G>C	ENSP00000409733.2:p.Gly282Arg
ENST00000613246.4:c.844G>C	ENSP00000477933.1:p.Gly282Arg
ENST00000615445.4:c.844G>C	ENSP00000479342.1:p.Gly282Arg
NM_001098503.1:c.844G>C	NP_001091973.1:p.Gly282Arg
NM_002843.3:c.844G>C	NP_002834.3:p.Gly282Arg
XM_011520249.1:c.877G>C	XP_011518551.1:p.Gly293Arg
XR_930883.1:n.1194G>C
XM_017018083.1:c.922G>C	XP_016873572.1:p.Gly308Arg
XM_017018084.1:c.865G>C	XP_016873573.1:p.Gly289Arg
XM_017018085.1:c.796G>C	XP_016873574.1:p.Gly266Arg
XR_930883.2:n.1253G>C
NM_002843.4:c.844G>C MANE Select	NP_002834.3:p.Gly282Arg
NM_001098503.2:c.844G>C	NP_001091973.1:p.Gly282Arg