Canonical Allele Identifier: CA474434530

Gene: PTPRJ

Linked Data

• gnomAD v4: 11-48123866-C-G
• MyVariant Identifiers: chr11:g.48145418C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123866C>G , CM000673.2:g.48123866C>G	GRCh38
NC_000011.9:g.48145418C>G , CM000673.1:g.48145418C>G	GRCh37
NC_000011.8:g.48101994C>G	NCBI36
NG_012209.1:g.148309C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1212C>G	ENSP00000514003.1:p.Gly404=
ENST00000418331.7:c.870C>G MANE Select	ENSP00000400010.2:p.Gly290=
ENST00000418331.6:c.870C>G	ENSP00000400010.2:p.Gly290=
ENST00000440289.6:c.870C>G	ENSP00000409733.2:p.Gly290=
ENST00000613246.4:c.870C>G	ENSP00000477933.1:p.Gly290=
ENST00000615445.4:c.870C>G	ENSP00000479342.1:p.Gly290=
NM_001098503.1:c.870C>G	NP_001091973.1:p.Gly290=
NM_002843.3:c.870C>G	NP_002834.3:p.Gly290=
XM_011520249.1:c.903C>G	XP_011518551.1:p.Gly301=
XR_930883.1:n.1220C>G
XM_017018083.1:c.948C>G	XP_016873572.1:p.Gly316=
XM_017018084.1:c.891C>G	XP_016873573.1:p.Gly297=
XM_017018085.1:c.822C>G	XP_016873574.1:p.Gly274=
XR_930883.2:n.1279C>G
NM_002843.4:c.870C>G MANE Select	NP_002834.3:p.Gly290=
NM_001098503.2:c.870C>G	NP_001091973.1:p.Gly290=