Canonical Allele Identifier: CA380369989

Gene: PTPRJ

Linked Data

• gnomAD v4: 11-48123658-G-A
• MyVariant Identifiers: chr11:g.48145210G>A (hg19) ; chr11:g.48123658G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123658G>A , CM000673.2:g.48123658G>A	GRCh38
NC_000011.9:g.48145210G>A , CM000673.1:g.48145210G>A	GRCh37
NC_000011.8:g.48101786G>A	NCBI36
NG_012209.1:g.148101G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1004G>A	ENSP00000514003.1:p.Arg335Lys
ENST00000418331.7:c.662G>A MANE Select	ENSP00000400010.2:p.Arg221Lys
ENST00000418331.6:c.662G>A	ENSP00000400010.2:p.Arg221Lys
ENST00000440289.6:c.662G>A	ENSP00000409733.2:p.Arg221Lys
ENST00000527952.1:c.398G>A	ENSP00000435618.1:p.Arg133Lys
ENST00000613246.4:c.662G>A	ENSP00000477933.1:p.Arg221Lys
ENST00000615445.4:c.662G>A	ENSP00000479342.1:p.Arg221Lys
NM_001098503.1:c.662G>A	NP_001091973.1:p.Arg221Lys
NM_002843.3:c.662G>A	NP_002834.3:p.Arg221Lys
XM_011520249.1:c.695G>A	XP_011518551.1:p.Arg232Lys
XR_930883.1:n.1012G>A
XM_017018083.1:c.740G>A	XP_016873572.1:p.Arg247Lys
XM_017018084.1:c.683G>A	XP_016873573.1:p.Arg228Lys
XM_017018085.1:c.614G>A	XP_016873574.1:p.Arg205Lys
XR_930883.2:n.1071G>A
NM_002843.4:c.662G>A MANE Select	NP_002834.3:p.Arg221Lys
NM_001098503.2:c.662G>A	NP_001091973.1:p.Arg221Lys