Canonical Allele Identifier: CA5982003

Gene: PTPRJ

Linked Data

• dbSNP Id: rs139028982
• ExAC: 11:48145380 A / G
• gnomAD v2: 11-48145380-A-G
• gnomAD v3: 11-48123828-A-G
• gnomAD v4: 11-48123828-A-G
• MyVariant Identifiers: chr11:g.48145380A>G (hg19) ; chr11:g.48123828A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123828A>G , CM000673.2:g.48123828A>G	GRCh38
NC_000011.9:g.48145380A>G , CM000673.1:g.48145380A>G	GRCh37
NC_000011.8:g.48101956A>G	NCBI36
NG_012209.1:g.148271A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698881.1:c.1174A>G	ENSP00000514003.1:p.Asn392Asp
ENST00000418331.7:c.832A>G MANE Select	ENSP00000400010.2:p.Asn278Asp
ENST00000418331.6:c.832A>G	ENSP00000400010.2:p.Asn278Asp
ENST00000440289.6:c.832A>G	ENSP00000409733.2:p.Asn278Asp
ENST00000613246.4:c.832A>G	ENSP00000477933.1:p.Asn278Asp
ENST00000615445.4:c.832A>G	ENSP00000479342.1:p.Asn278Asp
NM_001098503.1:c.832A>G	NP_001091973.1:p.Asn278Asp
NM_002843.3:c.832A>G	NP_002834.3:p.Asn278Asp
XM_011520249.1:c.865A>G	XP_011518551.1:p.Asn289Asp
XR_930883.1:n.1182A>G
XM_017018083.1:c.910A>G	XP_016873572.1:p.Asn304Asp
XM_017018084.1:c.853A>G	XP_016873573.1:p.Asn285Asp
XM_017018085.1:c.784A>G	XP_016873574.1:p.Asn262Asp
XR_930883.2:n.1241A>G
NM_002843.4:c.832A>G MANE Select	NP_002834.3:p.Asn278Asp
NM_001098503.2:c.832A>G	NP_001091973.1:p.Asn278Asp