Canonical Allele Identifier: CA380369851

Gene: PTPRJ

Linked Data

• COSMIC: COSM4033287 ; COSM4033288 ; COSM4033289
• MyVariant Identifiers: chr11:g.48145173C>A (hg19) ; chr11:g.48123621C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123621C>A , CM000673.2:g.48123621C>A	GRCh38
NC_000011.9:g.48145173C>A , CM000673.1:g.48145173C>A	GRCh37
NC_000011.8:g.48101749C>A	NCBI36
NG_012209.1:g.148064C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.967C>A	ENSP00000514003.1:p.Pro323Thr
ENST00000418331.7:c.625C>A MANE Select	ENSP00000400010.2:p.Pro209Thr
ENST00000418331.6:c.625C>A	ENSP00000400010.2:p.Pro209Thr
ENST00000440289.6:c.625C>A	ENSP00000409733.2:p.Pro209Thr
ENST00000527952.1:c.361C>A	ENSP00000435618.1:p.Pro121Thr
ENST00000613246.4:c.625C>A	ENSP00000477933.1:p.Pro209Thr
ENST00000615445.4:c.625C>A	ENSP00000479342.1:p.Pro209Thr
NM_001098503.1:c.625C>A	NP_001091973.1:p.Pro209Thr
NM_002843.3:c.625C>A	NP_002834.3:p.Pro209Thr
XM_011520249.1:c.658C>A	XP_011518551.1:p.Pro220Thr
XR_930883.1:n.975C>A
XM_017018083.1:c.703C>A	XP_016873572.1:p.Pro235Thr
XM_017018084.1:c.646C>A	XP_016873573.1:p.Pro216Thr
XM_017018085.1:c.577C>A	XP_016873574.1:p.Pro193Thr
XR_930883.2:n.1034C>A
NM_002843.4:c.625C>A MANE Select	NP_002834.3:p.Pro209Thr
NM_001098503.2:c.625C>A	NP_001091973.1:p.Pro209Thr