Canonical Allele Identifier: CA380370735

Gene: PTPRJ

Linked Data

• gnomAD v4: 11-48123835-C-T
• COSMIC: COSM1492602 ; COSM1492603
• MyVariant Identifiers: chr11:g.48145387C>T (hg19) ; chr11:g.48123835C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123835C>T , CM000673.2:g.48123835C>T	GRCh38
NC_000011.9:g.48145387C>T , CM000673.1:g.48145387C>T	GRCh37
NC_000011.8:g.48101963C>T	NCBI36
NG_012209.1:g.148278C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1181C>T	ENSP00000514003.1:p.Thr394Ile
ENST00000418331.7:c.839C>T MANE Select	ENSP00000400010.2:p.Thr280Ile
ENST00000418331.6:c.839C>T	ENSP00000400010.2:p.Thr280Ile
ENST00000440289.6:c.839C>T	ENSP00000409733.2:p.Thr280Ile
ENST00000613246.4:c.839C>T	ENSP00000477933.1:p.Thr280Ile
ENST00000615445.4:c.839C>T	ENSP00000479342.1:p.Thr280Ile
NM_001098503.1:c.839C>T	NP_001091973.1:p.Thr280Ile
NM_002843.3:c.839C>T	NP_002834.3:p.Thr280Ile
XM_011520249.1:c.872C>T	XP_011518551.1:p.Thr291Ile
XR_930883.1:n.1189C>T
XM_017018083.1:c.917C>T	XP_016873572.1:p.Thr306Ile
XM_017018084.1:c.860C>T	XP_016873573.1:p.Thr287Ile
XM_017018085.1:c.791C>T	XP_016873574.1:p.Thr264Ile
XR_930883.2:n.1248C>T
NM_002843.4:c.839C>T MANE Select	NP_002834.3:p.Thr280Ile
NM_001098503.2:c.839C>T	NP_001091973.1:p.Thr280Ile