Canonical Allele Identifier: CA5981977

Gene: PTPRJ

Linked Data

• dbSNP Id: rs777464558
• ExAC: 11:48145236 G / A
• gnomAD v2: 11-48145236-G-A
• gnomAD v3: 11-48123684-G-A
• gnomAD v4: 11-48123684-G-A
• MyVariant Identifiers: chr11:g.48145236G>A (hg19) ; chr11:g.48123684G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123684G>A , CM000673.2:g.48123684G>A	GRCh38
NC_000011.9:g.48145236G>A , CM000673.1:g.48145236G>A	GRCh37
NC_000011.8:g.48101812G>A	NCBI36
NG_012209.1:g.148127G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1030G>A	ENSP00000514003.1:p.Gly344Ser
ENST00000418331.7:c.688G>A MANE Select	ENSP00000400010.2:p.Gly230Ser
ENST00000418331.6:c.688G>A	ENSP00000400010.2:p.Gly230Ser
ENST00000440289.6:c.688G>A	ENSP00000409733.2:p.Gly230Ser
ENST00000527952.1:c.424G>A	ENSP00000435618.1:p.Gly142Ser
ENST00000613246.4:c.688G>A	ENSP00000477933.1:p.Gly230Ser
ENST00000615445.4:c.688G>A	ENSP00000479342.1:p.Gly230Ser
NM_001098503.1:c.688G>A	NP_001091973.1:p.Gly230Ser
NM_002843.3:c.688G>A	NP_002834.3:p.Gly230Ser
XM_011520249.1:c.721G>A	XP_011518551.1:p.Gly241Ser
XR_930883.1:n.1038G>A
XM_017018083.1:c.766G>A	XP_016873572.1:p.Gly256Ser
XM_017018084.1:c.709G>A	XP_016873573.1:p.Gly237Ser
XM_017018085.1:c.640G>A	XP_016873574.1:p.Gly214Ser
XR_930883.2:n.1097G>A
NM_002843.4:c.688G>A MANE Select	NP_002834.3:p.Gly230Ser
NM_001098503.2:c.688G>A	NP_001091973.1:p.Gly230Ser