Canonical Allele Identifier: CA380370747
Gene: PTPRJ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.48123838A>G , CM000673.2:g.48123838A>G GRCh38
NC_000011.9:g.48145390A>G , CM000673.1:g.48145390A>G GRCh37
NC_000011.8:g.48101966A>G NCBI36
NG_012209.1:g.148281A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698881.1:c.1184A>G ENSP00000514003.1:p.Lys395Arg
ENST00000418331.7:c.842A>G MANE Select ENSP00000400010.2:p.Lys281Arg
ENST00000418331.6:c.842A>G ENSP00000400010.2:p.Lys281Arg
ENST00000440289.6:c.842A>G ENSP00000409733.2:p.Lys281Arg
ENST00000613246.4:c.842A>G ENSP00000477933.1:p.Lys281Arg
ENST00000615445.4:c.842A>G ENSP00000479342.1:p.Lys281Arg
NM_001098503.1:c.842A>G NP_001091973.1:p.Lys281Arg
NM_002843.3:c.842A>G NP_002834.3:p.Lys281Arg
XM_011520249.1:c.875A>G XP_011518551.1:p.Lys292Arg
XR_930883.1:n.1192A>G
XM_017018083.1:c.920A>G XP_016873572.1:p.Lys307Arg
XM_017018084.1:c.863A>G XP_016873573.1:p.Lys288Arg
XM_017018085.1:c.794A>G XP_016873574.1:p.Lys265Arg
XR_930883.2:n.1251A>G
NM_002843.4:c.842A>G MANE Select NP_002834.3:p.Lys281Arg
NM_001098503.2:c.842A>G NP_001091973.1:p.Lys281Arg