Canonical Allele Identifier: CA380370115

Gene: PTPRJ

Linked Data

• dbSNP Id: rs1412825912
• gnomAD v2: 11-48145240-A-G
• gnomAD v4: 11-48123688-A-G
• MyVariant Identifiers: chr11:g.48145240A>G (hg19) ; chr11:g.48123688A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123688A>G , CM000673.2:g.48123688A>G	GRCh38
NC_000011.9:g.48145240A>G , CM000673.1:g.48145240A>G	GRCh37
NC_000011.8:g.48101816A>G	NCBI36
NG_012209.1:g.148131A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1034A>G	ENSP00000514003.1:p.Asn345Ser
ENST00000418331.7:c.692A>G MANE Select	ENSP00000400010.2:p.Asn231Ser
ENST00000418331.6:c.692A>G	ENSP00000400010.2:p.Asn231Ser
ENST00000440289.6:c.692A>G	ENSP00000409733.2:p.Asn231Ser
ENST00000527952.1:c.428A>G	ENSP00000435618.1:p.Asn143Ser
ENST00000613246.4:c.692A>G	ENSP00000477933.1:p.Asn231Ser
ENST00000615445.4:c.692A>G	ENSP00000479342.1:p.Asn231Ser
NM_001098503.1:c.692A>G	NP_001091973.1:p.Asn231Ser
NM_002843.3:c.692A>G	NP_002834.3:p.Asn231Ser
XM_011520249.1:c.725A>G	XP_011518551.1:p.Asn242Ser
XR_930883.1:n.1042A>G
XM_017018083.1:c.770A>G	XP_016873572.1:p.Asn257Ser
XM_017018084.1:c.713A>G	XP_016873573.1:p.Asn238Ser
XM_017018085.1:c.644A>G	XP_016873574.1:p.Asn215Ser
XR_930883.2:n.1101A>G
NM_002843.4:c.692A>G MANE Select	NP_002834.3:p.Asn231Ser
NM_001098503.2:c.692A>G	NP_001091973.1:p.Asn231Ser