Canonical Allele Identifier: CA1969701908

Gene: PTPRJ

Linked Data

• dbSNP Id: rs1856772582
• gnomAD v3: 11-48123909-T-A
• gnomAD v4: 11-48123909-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.48123909T>A , CM000673.2:g.48123909T>A	GRCh38
NC_000011.9:g.48145461T>A , CM000673.1:g.48145461T>A	GRCh37
NC_000011.8:g.48102037T>A	NCBI36
NG_012209.1:g.148352T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698881.1:c.1216+39T>A	ENSP00000514003.1:n.1216+39T>A
ENST00000418331.7:c.874+39T>A MANE Select	ENSP00000400010.2:n.874+39T>A
ENST00000418331.6:c.874+39T>A	ENSP00000400010.2:n.874+39T>A
ENST00000440289.6:c.874+39T>A	ENSP00000409733.2:n.874+39T>A
ENST00000613246.4:c.874+39T>A	ENSP00000477933.1:n.874+39T>A
ENST00000615445.4:c.874+39T>A	ENSP00000479342.1:n.874+39T>A
NM_001098503.1:c.874+39T>A	NP_001091973.1:n.874+39T>A
NM_002843.3:c.874+39T>A	NP_002834.3:n.874+39T>A
XM_011520249.1:c.907+39T>A	XP_011518551.1:n.907+39T>A
XR_930883.1:n.1224+39T>A
XM_017018083.1:c.952+39T>A	XP_016873572.1:n.952+39T>A
XM_017018084.1:c.895+39T>A	XP_016873573.1:n.895+39T>A
XM_017018085.1:c.826+39T>A	XP_016873574.1:n.826+39T>A
XR_930883.2:n.1283+39T>A
NM_002843.4:c.874+39T>A MANE Select	NP_002834.3:n.874+39T>A
NM_001098503.2:c.874+39T>A	NP_001091973.1:n.874+39T>A