Canonical Allele Identifier: CA1969701814
Gene: PTPRJ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.48123826C= , CM000673.2:g.48123826C= GRCh38
NC_000011.9:g.48145378C= , CM000673.1:g.48145378C= GRCh37
NC_000011.8:g.48101954C= NCBI36
NG_012209.1:g.148269C=

Transcript Alleles

HGVS Amino-acid change
ENST00000698881.1:c.1172C= ENSP00000514003.1:p.Ser391=
ENST00000418331.7:c.830C= MANE Select ENSP00000400010.2:p.Ser277=
ENST00000418331.6:c.830C= ENSP00000400010.2:p.Ser277=
ENST00000440289.6:c.830C= ENSP00000409733.2:p.Ser277=
ENST00000613246.4:c.830C= ENSP00000477933.1:p.Ser277=
ENST00000615445.4:c.830C= ENSP00000479342.1:p.Ser277=
NM_001098503.1:c.830C= NP_001091973.1:p.Ser277=
NM_002843.3:c.830C= NP_002834.3:p.Ser277=
XM_011520249.1:c.863C= XP_011518551.1:p.Ser288=
XR_930883.1:n.1180C=
XM_017018083.1:c.908C= XP_016873572.1:p.Ser303=
XM_017018084.1:c.851C= XP_016873573.1:p.Ser284=
XM_017018085.1:c.782C= XP_016873574.1:p.Ser261=
XR_930883.2:n.1239C=
NM_002843.4:c.830C= MANE Select NP_002834.3:p.Ser277=
NM_001098503.2:c.830C= NP_001091973.1:p.Ser277=