Canonical Allele Identifier: CA599088619

Gene: PTPRJ

Linked Data

• dbSNP Id: rs1220719904
• gnomAD v2: 11-48144836-TA-T
• gnomAD v3: 11-48123284-TA-T
• gnomAD v4: 11-48123284-TA-T
• MyVariant Identifiers: chr11:g.48144837del (hg19) ; chr11:g.48123285del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123288del , CM000673.2:g.48123288del	GRCh38
NC_000011.9:g.48144840del , CM000673.1:g.48144840del	GRCh37
NC_000011.8:g.48101416del	NCBI36
NG_012209.1:g.147731del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.959-325del	ENSP00000514003.1:n.959-325del
ENST00000418331.7:c.617-325del MANE Select	ENSP00000400010.2:n.617-325del
ENST00000418331.6:c.617-325del	ENSP00000400010.2:n.617-325del
ENST00000440289.6:c.617-325del	ENSP00000409733.2:n.617-325del
ENST00000527952.1:c.353-325del	ENSP00000435618.1:n.353-325del
ENST00000613246.4:c.617-325del	ENSP00000477933.1:n.617-325del
ENST00000615445.4:c.617-325del	ENSP00000479342.1:n.617-325del
NM_001098503.1:c.617-325del	NP_001091973.1:n.617-325del
NM_002843.3:c.617-325del	NP_002834.3:n.617-325del
XM_011520249.1:c.650-325del	XP_011518551.1:n.650-325del
XR_930883.1:n.967-325del
XM_017018083.1:c.695-325del	XP_016873572.1:n.695-325del
XM_017018084.1:c.638-325del	XP_016873573.1:n.638-325del
XM_017018085.1:c.569-325del	XP_016873574.1:n.569-325del
XR_930883.2:n.1026-325del
NM_002843.4:c.617-325del MANE Select	NP_002834.3:n.617-325del
NM_001098503.2:c.617-325del	NP_001091973.1:n.617-325del