Canonical Allele Identifier: CA221746899

Gene: PTPRJ

Linked Data

• dbSNP Id: rs1037666641
• gnomAD v2: 11-48145189-G-A
• gnomAD v4: 11-48123637-G-A
• MyVariant Identifiers: chr11:g.48145189G>A (hg19) ; chr11:g.48123637G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123637G>A , CM000673.2:g.48123637G>A	GRCh38
NC_000011.9:g.48145189G>A , CM000673.1:g.48145189G>A	GRCh37
NC_000011.8:g.48101765G>A	NCBI36
NG_012209.1:g.148080G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.983G>A	ENSP00000514003.1:p.Arg328His
ENST00000418331.7:c.641G>A MANE Select	ENSP00000400010.2:p.Arg214His
ENST00000418331.6:c.641G>A	ENSP00000400010.2:p.Arg214His
ENST00000440289.6:c.641G>A	ENSP00000409733.2:p.Arg214His
ENST00000527952.1:c.377G>A	ENSP00000435618.1:p.Arg126His
ENST00000613246.4:c.641G>A	ENSP00000477933.1:p.Arg214His
ENST00000615445.4:c.641G>A	ENSP00000479342.1:p.Arg214His
NM_001098503.1:c.641G>A	NP_001091973.1:p.Arg214His
NM_002843.3:c.641G>A	NP_002834.3:p.Arg214His
XM_011520249.1:c.674G>A	XP_011518551.1:p.Arg225His
XR_930883.1:n.991G>A
XM_017018083.1:c.719G>A	XP_016873572.1:p.Arg240His
XM_017018084.1:c.662G>A	XP_016873573.1:p.Arg221His
XM_017018085.1:c.593G>A	XP_016873574.1:p.Arg198His
XR_930883.2:n.1050G>A
NM_002843.4:c.641G>A MANE Select	NP_002834.3:p.Arg214His
NM_001098503.2:c.641G>A	NP_001091973.1:p.Arg214His