Canonical Allele Identifier: CA380370456

Gene: PTPRJ

Linked Data

• gnomAD v4: 11-48123777-G-T
• MyVariant Identifiers: chr11:g.48145329G>T (hg19) ; chr11:g.48123777G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123777G>T , CM000673.2:g.48123777G>T	GRCh38
NC_000011.9:g.48145329G>T , CM000673.1:g.48145329G>T	GRCh37
NC_000011.8:g.48101905G>T	NCBI36
NG_012209.1:g.148220G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1123G>T	ENSP00000514003.1:p.Gly375Cys
ENST00000418331.7:c.781G>T MANE Select	ENSP00000400010.2:p.Gly261Cys
ENST00000418331.6:c.781G>T	ENSP00000400010.2:p.Gly261Cys
ENST00000440289.6:c.781G>T	ENSP00000409733.2:p.Gly261Cys
ENST00000613246.4:c.781G>T	ENSP00000477933.1:p.Gly261Cys
ENST00000615445.4:c.781G>T	ENSP00000479342.1:p.Gly261Cys
NM_001098503.1:c.781G>T	NP_001091973.1:p.Gly261Cys
NM_002843.3:c.781G>T	NP_002834.3:p.Gly261Cys
XM_011520249.1:c.814G>T	XP_011518551.1:p.Gly272Cys
XR_930883.1:n.1131G>T
XM_017018083.1:c.859G>T	XP_016873572.1:p.Gly287Cys
XM_017018084.1:c.802G>T	XP_016873573.1:p.Gly268Cys
XM_017018085.1:c.733G>T	XP_016873574.1:p.Gly245Cys
XR_930883.2:n.1190G>T
NM_002843.4:c.781G>T MANE Select	NP_002834.3:p.Gly261Cys
NM_001098503.2:c.781G>T	NP_001091973.1:p.Gly261Cys