Canonical Allele Identifier: CA599375851

Gene: PTPRJ

Linked Data

• dbSNP Id: rs1249038831
• gnomAD v2: 11-48145514-T-G
• gnomAD v3: 11-48123962-T-G
• gnomAD v4: 11-48123962-T-G
• MyVariant Identifiers: chr11:g.48145514T>G (hg19) ; chr11:g.48123962T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123962T>G , CM000673.2:g.48123962T>G	GRCh38
NC_000011.9:g.48145514T>G , CM000673.1:g.48145514T>G	GRCh37
NC_000011.8:g.48102090T>G	NCBI36
NG_012209.1:g.148405T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1216+92T>G	ENSP00000514003.1:n.1216+92T>G
ENST00000418331.7:c.874+92T>G MANE Select	ENSP00000400010.2:n.874+92T>G
ENST00000418331.6:c.874+92T>G	ENSP00000400010.2:n.874+92T>G
ENST00000440289.6:c.874+92T>G	ENSP00000409733.2:n.874+92T>G
ENST00000613246.4:c.874+92T>G	ENSP00000477933.1:n.874+92T>G
ENST00000615445.4:c.874+92T>G	ENSP00000479342.1:n.874+92T>G
NM_001098503.1:c.874+92T>G	NP_001091973.1:n.874+92T>G
NM_002843.3:c.874+92T>G	NP_002834.3:n.874+92T>G
XM_011520249.1:c.907+92T>G	XP_011518551.1:n.907+92T>G
XR_930883.1:n.1224+92T>G
XM_017018083.1:c.952+92T>G	XP_016873572.1:n.952+92T>G
XM_017018084.1:c.895+92T>G	XP_016873573.1:n.895+92T>G
XM_017018085.1:c.826+92T>G	XP_016873574.1:n.826+92T>G
XR_930883.2:n.1283+92T>G
NM_002843.4:c.874+92T>G MANE Select	NP_002834.3:n.874+92T>G
NM_001098503.2:c.874+92T>G	NP_001091973.1:n.874+92T>G