Canonical Allele Identifier: CA5981967
Gene: PTPRJ HGNC NCBI

Linked Data

dbSNP Id: rs777121066

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.48123622C>T , CM000673.2:g.48123622C>T GRCh38
NC_000011.9:g.48145174C>T , CM000673.1:g.48145174C>T GRCh37
NC_000011.8:g.48101750C>T NCBI36
NG_012209.1:g.148065C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698881.1:c.968C>T ENSP00000514003.1:p.Pro323Leu
ENST00000418331.7:c.626C>T MANE Select ENSP00000400010.2:p.Pro209Leu
ENST00000418331.6:c.626C>T ENSP00000400010.2:p.Pro209Leu
ENST00000440289.6:c.626C>T ENSP00000409733.2:p.Pro209Leu
ENST00000527952.1:c.362C>T ENSP00000435618.1:p.Pro121Leu
ENST00000613246.4:c.626C>T ENSP00000477933.1:p.Pro209Leu
ENST00000615445.4:c.626C>T ENSP00000479342.1:p.Pro209Leu
NM_001098503.1:c.626C>T NP_001091973.1:p.Pro209Leu
NM_002843.3:c.626C>T NP_002834.3:p.Pro209Leu
XM_011520249.1:c.659C>T XP_011518551.1:p.Pro220Leu
XR_930883.1:n.976C>T
XM_017018083.1:c.704C>T XP_016873572.1:p.Pro235Leu
XM_017018084.1:c.647C>T XP_016873573.1:p.Pro216Leu
XM_017018085.1:c.578C>T XP_016873574.1:p.Pro193Leu
XR_930883.2:n.1035C>T
NM_002843.4:c.626C>T MANE Select NP_002834.3:p.Pro209Leu
NM_001098503.2:c.626C>T NP_001091973.1:p.Pro209Leu