Canonical Allele Identifier: CA677101834

Gene: PTPRJ

Linked Data

• dbSNP Id: rs1186892604
• gnomAD v3: 11-48123276-CTA-C
• gnomAD v4: 11-48123276-CTA-C
• MyVariant Identifiers: chr11:g.48144829_48144830del (hg19) ; chr11:g.48123277_48123278del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123277_48123278del , CM000673.2:g.48123277_48123278del	GRCh38
NC_000011.9:g.48144829_48144830del , CM000673.1:g.48144829_48144830del	GRCh37
NC_000011.8:g.48101405_48101406del	NCBI36
NG_012209.1:g.147720_147721del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.959-336_959-335del	ENSP00000514003.1:n.959-336_959-335del
ENST00000418331.7:c.617-336_617-335del MANE Select	ENSP00000400010.2:n.617-336_617-335del
ENST00000418331.6:c.617-336_617-335del	ENSP00000400010.2:n.617-336_617-335del
ENST00000440289.6:c.617-336_617-335del	ENSP00000409733.2:n.617-336_617-335del
ENST00000527952.1:c.353-336_353-335del	ENSP00000435618.1:n.353-336_353-335del
ENST00000613246.4:c.617-336_617-335del	ENSP00000477933.1:n.617-336_617-335del
ENST00000615445.4:c.617-336_617-335del	ENSP00000479342.1:n.617-336_617-335del
NM_001098503.1:c.617-336_617-335del	NP_001091973.1:n.617-336_617-335del
NM_002843.3:c.617-336_617-335del	NP_002834.3:n.617-336_617-335del
XM_011520249.1:c.650-336_650-335del	XP_011518551.1:n.650-336_650-335del
XR_930883.1:n.967-336_967-335del
XM_017018083.1:c.695-336_695-335del	XP_016873572.1:n.695-336_695-335del
XM_017018084.1:c.638-336_638-335del	XP_016873573.1:n.638-336_638-335del
XM_017018085.1:c.569-336_569-335del	XP_016873574.1:n.569-336_569-335del
XR_930883.2:n.1026-336_1026-335del
NM_002843.4:c.617-336_617-335del MANE Select	NP_002834.3:n.617-336_617-335del
NM_001098503.2:c.617-336_617-335del	NP_001091973.1:n.617-336_617-335del