Canonical Allele Identifier: CA380370731
Gene: PTPRJ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.48123834A>T , CM000673.2:g.48123834A>T GRCh38
NC_000011.9:g.48145386A>T , CM000673.1:g.48145386A>T GRCh37
NC_000011.8:g.48101962A>T NCBI36
NG_012209.1:g.148277A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698881.1:c.1180A>T ENSP00000514003.1:p.Thr394Ser
ENST00000418331.7:c.838A>T MANE Select ENSP00000400010.2:p.Thr280Ser
ENST00000418331.6:c.838A>T ENSP00000400010.2:p.Thr280Ser
ENST00000440289.6:c.838A>T ENSP00000409733.2:p.Thr280Ser
ENST00000613246.4:c.838A>T ENSP00000477933.1:p.Thr280Ser
ENST00000615445.4:c.838A>T ENSP00000479342.1:p.Thr280Ser
NM_001098503.1:c.838A>T NP_001091973.1:p.Thr280Ser
NM_002843.3:c.838A>T NP_002834.3:p.Thr280Ser
XM_011520249.1:c.871A>T XP_011518551.1:p.Thr291Ser
XR_930883.1:n.1188A>T
XM_017018083.1:c.916A>T XP_016873572.1:p.Thr306Ser
XM_017018084.1:c.859A>T XP_016873573.1:p.Thr287Ser
XM_017018085.1:c.790A>T XP_016873574.1:p.Thr264Ser
XR_930883.2:n.1247A>T
NM_002843.4:c.838A>T MANE Select NP_002834.3:p.Thr280Ser
NM_001098503.2:c.838A>T NP_001091973.1:p.Thr280Ser