Canonical Allele Identifier: CA2613454285
Gene: PTPRJ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.48123890_48123891insGCCC , CM000673.2:g.48123890_48123891insGCCC GRCh38
NC_000011.9:g.48145442_48145443insGCCC , CM000673.1:g.48145442_48145443insGCCC GRCh37
NC_000011.8:g.48102018_48102019insGCCC NCBI36
NG_012209.1:g.148333_148334insGCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000698881.1:c.1216+20_1216+21insGCCC ENSP00000514003.1:n.1216+20_1216+21insGCCC
ENST00000418331.7:c.874+20_874+21insGCCC MANE Select ENSP00000400010.2:n.874+20_874+21insGCCC
ENST00000418331.6:c.874+20_874+21insGCCC ENSP00000400010.2:n.874+20_874+21insGCCC
ENST00000440289.6:c.874+20_874+21insGCCC ENSP00000409733.2:n.874+20_874+21insGCCC
ENST00000613246.4:c.874+20_874+21insGCCC ENSP00000477933.1:n.874+20_874+21insGCCC
ENST00000615445.4:c.874+20_874+21insGCCC ENSP00000479342.1:n.874+20_874+21insGCCC
NM_001098503.1:c.874+20_874+21insGCCC NP_001091973.1:n.874+20_874+21insGCCC
NM_002843.3:c.874+20_874+21insGCCC NP_002834.3:n.874+20_874+21insGCCC
XM_011520249.1:c.907+20_907+21insGCCC XP_011518551.1:n.907+20_907+21insGCCC
XR_930883.1:n.1224+20_1224+21insGCCC
XM_017018083.1:c.952+20_952+21insGCCC XP_016873572.1:n.952+20_952+21insGCCC
XM_017018084.1:c.895+20_895+21insGCCC XP_016873573.1:n.895+20_895+21insGCCC
XM_017018085.1:c.826+20_826+21insGCCC XP_016873574.1:n.826+20_826+21insGCCC
XR_930883.2:n.1283+20_1283+21insGCCC
NM_002843.4:c.874+20_874+21insGCCC MANE Select NP_002834.3:n.874+20_874+21insGCCC
NM_001098503.2:c.874+20_874+21insGCCC NP_001091973.1:n.874+20_874+21insGCCC