Canonical Allele Identifier: CA474434396

Gene: PTPRJ

Linked Data

• MyVariant Identifiers: chr11:g.48145313T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123761T>A , CM000673.2:g.48123761T>A	GRCh38
NC_000011.9:g.48145313T>A , CM000673.1:g.48145313T>A	GRCh37
NC_000011.8:g.48101889T>A	NCBI36
NG_012209.1:g.148204T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1107T>A	ENSP00000514003.1:p.Leu369=
ENST00000418331.7:c.765T>A MANE Select	ENSP00000400010.2:p.Leu255=
ENST00000418331.6:c.765T>A	ENSP00000400010.2:p.Leu255=
ENST00000440289.6:c.765T>A	ENSP00000409733.2:p.Leu255=
ENST00000613246.4:c.765T>A	ENSP00000477933.1:p.Leu255=
ENST00000615445.4:c.765T>A	ENSP00000479342.1:p.Leu255=
NM_001098503.1:c.765T>A	NP_001091973.1:p.Leu255=
NM_002843.3:c.765T>A	NP_002834.3:p.Leu255=
XM_011520249.1:c.798T>A	XP_011518551.1:p.Leu266=
XR_930883.1:n.1115T>A
XM_017018083.1:c.843T>A	XP_016873572.1:p.Leu281=
XM_017018084.1:c.786T>A	XP_016873573.1:p.Leu262=
XM_017018085.1:c.717T>A	XP_016873574.1:p.Leu239=
XR_930883.2:n.1174T>A
NM_002843.4:c.765T>A MANE Select	NP_002834.3:p.Leu255=
NM_001098503.2:c.765T>A	NP_001091973.1:p.Leu255=