Canonical Allele Identifier: CA380369812

Gene: PTPRJ

Linked Data

• COSMIC: COSM3980352 ; COSM3980353 ; COSM3980354
• MyVariant Identifiers: chr11:g.48145165A>G (hg19) ; chr11:g.48123613A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123613A>G , CM000673.2:g.48123613A>G	GRCh38
NC_000011.9:g.48145165A>G , CM000673.1:g.48145165A>G	GRCh37
NC_000011.8:g.48101741A>G	NCBI36
NG_012209.1:g.148056A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.959A>G	ENSP00000514003.1:p.Glu320Gly
ENST00000418331.7:c.617A>G MANE Select	ENSP00000400010.2:p.Glu206Gly
ENST00000418331.6:c.617A>G	ENSP00000400010.2:p.Glu206Gly
ENST00000440289.6:c.617A>G	ENSP00000409733.2:p.Glu206Gly
ENST00000527952.1:c.353A>G	ENSP00000435618.1:p.Glu118Gly
ENST00000613246.4:c.617A>G	ENSP00000477933.1:p.Glu206Gly
ENST00000615445.4:c.617A>G	ENSP00000479342.1:p.Glu206Gly
NM_001098503.1:c.617A>G	NP_001091973.1:p.Glu206Gly
NM_002843.3:c.617A>G	NP_002834.3:p.Glu206Gly
XM_011520249.1:c.650A>G	XP_011518551.1:p.Glu217Gly
XR_930883.1:n.967A>G
XM_017018083.1:c.695A>G	XP_016873572.1:p.Glu232Gly
XM_017018084.1:c.638A>G	XP_016873573.1:p.Glu213Gly
XM_017018085.1:c.569A>G	XP_016873574.1:p.Glu190Gly
XR_930883.2:n.1026A>G
NM_002843.4:c.617A>G MANE Select	NP_002834.3:p.Glu206Gly
NM_001098503.2:c.617A>G	NP_001091973.1:p.Glu206Gly