Canonical Allele Identifier: CA2613454262

Gene: PTPRJ

Linked Data

• gnomAD v4: 11-48123602-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123602T>A , CM000673.2:g.48123602T>A	GRCh38
NC_000011.9:g.48145154T>A , CM000673.1:g.48145154T>A	GRCh37
NC_000011.8:g.48101730T>A	NCBI36
NG_012209.1:g.148045T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.959-11T>A	ENSP00000514003.1:n.959-11T>A
ENST00000418331.7:c.617-11T>A MANE Select	ENSP00000400010.2:n.617-11T>A
ENST00000418331.6:c.617-11T>A	ENSP00000400010.2:n.617-11T>A
ENST00000440289.6:c.617-11T>A	ENSP00000409733.2:n.617-11T>A
ENST00000527952.1:c.353-11T>A	ENSP00000435618.1:n.353-11T>A
ENST00000613246.4:c.617-11T>A	ENSP00000477933.1:n.617-11T>A
ENST00000615445.4:c.617-11T>A	ENSP00000479342.1:n.617-11T>A
NM_001098503.1:c.617-11T>A	NP_001091973.1:n.617-11T>A
NM_002843.3:c.617-11T>A	NP_002834.3:n.617-11T>A
XM_011520249.1:c.650-11T>A	XP_011518551.1:n.650-11T>A
XR_930883.1:n.967-11T>A
XM_017018083.1:c.695-11T>A	XP_016873572.1:n.695-11T>A
XM_017018084.1:c.638-11T>A	XP_016873573.1:n.638-11T>A
XM_017018085.1:c.569-11T>A	XP_016873574.1:n.569-11T>A
XR_930883.2:n.1026-11T>A
NM_002843.4:c.617-11T>A MANE Select	NP_002834.3:n.617-11T>A
NM_001098503.2:c.617-11T>A	NP_001091973.1:n.617-11T>A