Canonical Allele Identifier: CA380369984

Gene: PTPRJ

Linked Data

• gnomAD v4: 11-48123657-A-G
• COSMIC: COSM6360704 ; COSM6360705 ; COSM6360706
• MyVariant Identifiers: chr11:g.48145209A>G (hg19) ; chr11:g.48123657A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123657A>G , CM000673.2:g.48123657A>G	GRCh38
NC_000011.9:g.48145209A>G , CM000673.1:g.48145209A>G	GRCh37
NC_000011.8:g.48101785A>G	NCBI36
NG_012209.1:g.148100A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1003A>G	ENSP00000514003.1:p.Arg335Gly
ENST00000418331.7:c.661A>G MANE Select	ENSP00000400010.2:p.Arg221Gly
ENST00000418331.6:c.661A>G	ENSP00000400010.2:p.Arg221Gly
ENST00000440289.6:c.661A>G	ENSP00000409733.2:p.Arg221Gly
ENST00000527952.1:c.397A>G	ENSP00000435618.1:p.Arg133Gly
ENST00000613246.4:c.661A>G	ENSP00000477933.1:p.Arg221Gly
ENST00000615445.4:c.661A>G	ENSP00000479342.1:p.Arg221Gly
NM_001098503.1:c.661A>G	NP_001091973.1:p.Arg221Gly
NM_002843.3:c.661A>G	NP_002834.3:p.Arg221Gly
XM_011520249.1:c.694A>G	XP_011518551.1:p.Arg232Gly
XR_930883.1:n.1011A>G
XM_017018083.1:c.739A>G	XP_016873572.1:p.Arg247Gly
XM_017018084.1:c.682A>G	XP_016873573.1:p.Arg228Gly
XM_017018085.1:c.613A>G	XP_016873574.1:p.Arg205Gly
XR_930883.2:n.1070A>G
NM_002843.4:c.661A>G MANE Select	NP_002834.3:p.Arg221Gly
NM_001098503.2:c.661A>G	NP_001091973.1:p.Arg221Gly