Canonical Allele Identifier: CA474434519

Gene: PTPRJ

Linked Data

• gnomAD v4: 11-48123854-C-A
• MyVariant Identifiers: chr11:g.48145406C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123854C>A , CM000673.2:g.48123854C>A	GRCh38
NC_000011.9:g.48145406C>A , CM000673.1:g.48145406C>A	GRCh37
NC_000011.8:g.48101982C>A	NCBI36
NG_012209.1:g.148297C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1200C>A	ENSP00000514003.1:p.Gly400=
ENST00000418331.7:c.858C>A MANE Select	ENSP00000400010.2:p.Gly286=
ENST00000418331.6:c.858C>A	ENSP00000400010.2:p.Gly286=
ENST00000440289.6:c.858C>A	ENSP00000409733.2:p.Gly286=
ENST00000613246.4:c.858C>A	ENSP00000477933.1:p.Gly286=
ENST00000615445.4:c.858C>A	ENSP00000479342.1:p.Gly286=
NM_001098503.1:c.858C>A	NP_001091973.1:p.Gly286=
NM_002843.3:c.858C>A	NP_002834.3:p.Gly286=
XM_011520249.1:c.891C>A	XP_011518551.1:p.Gly297=
XR_930883.1:n.1208C>A
XM_017018083.1:c.936C>A	XP_016873572.1:p.Gly312=
XM_017018084.1:c.879C>A	XP_016873573.1:p.Gly293=
XM_017018085.1:c.810C>A	XP_016873574.1:p.Gly270=
XR_930883.2:n.1267C>A
NM_002843.4:c.858C>A MANE Select	NP_002834.3:p.Gly286=
NM_001098503.2:c.858C>A	NP_001091973.1:p.Gly286=