Canonical Allele Identifier: CA380370169

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145255G>A (hg19) ; chr11:g.48123703G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123703G>A , CM000673.2:g.48123703G>A	GRCh38
NC_000011.9:g.48145255G>A , CM000673.1:g.48145255G>A	GRCh37
NC_000011.8:g.48101831G>A	NCBI36
NG_012209.1:g.148146G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1049G>A	ENSP00000514003.1:p.Cys350Tyr
ENST00000418331.7:c.707G>A MANE Select	ENSP00000400010.2:p.Cys236Tyr
ENST00000418331.6:c.707G>A	ENSP00000400010.2:p.Cys236Tyr
ENST00000440289.6:c.707G>A	ENSP00000409733.2:p.Cys236Tyr
ENST00000613246.4:c.707G>A	ENSP00000477933.1:p.Cys236Tyr
ENST00000615445.4:c.707G>A	ENSP00000479342.1:p.Cys236Tyr
NM_001098503.1:c.707G>A	NP_001091973.1:p.Cys236Tyr
NM_002843.3:c.707G>A	NP_002834.3:p.Cys236Tyr
XM_011520249.1:c.740G>A	XP_011518551.1:p.Cys247Tyr
XR_930883.1:n.1057G>A
XM_017018083.1:c.785G>A	XP_016873572.1:p.Cys262Tyr
XM_017018084.1:c.728G>A	XP_016873573.1:p.Cys243Tyr
XM_017018085.1:c.659G>A	XP_016873574.1:p.Cys220Tyr
XR_930883.2:n.1116G>A
NM_002843.4:c.707G>A MANE Select	NP_002834.3:p.Cys236Tyr
NM_001098503.2:c.707G>A	NP_001091973.1:p.Cys236Tyr