Canonical Allele Identifier: CA1955758475
Gene: PTPN5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.18783387A>T , CM000673.2:g.18783387A>T GRCh38
NC_000011.9:g.18804934A>T , CM000673.1:g.18804934A>T GRCh37
NC_000011.8:g.18761510A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000358540.7:c.-114+8138T>A MANE Select ENSP00000351342.2:n.-114+8138T>A
ENST00000358540.6:c.-114+8138T>A ENSP00000351342.2:n.-114+8138T>A
ENST00000396168.1:c.-53+8138T>A ENSP00000379471.1:n.-53+8138T>A
ENST00000396170.5:c.-69+8138T>A ENSP00000379473.1:n.-69+8138T>A
NM_001039970.1:c.-114+8138T>A NP_001035059.1:n.-114+8138T>A
NM_001278236.1:c.-69+8138T>A NP_001265165.1:n.-69+8138T>A
NM_001278238.1:c.-53+8138T>A NP_001265167.1:n.-53+8138T>A
NM_001278239.1:c.-53+8138T>A NP_001265168.1:n.-53+8138T>A
NM_006906.1:c.-114+8138T>A NP_008837.1:n.-114+8138T>A
NM_032781.3:c.-69+8138T>A NP_116170.3:n.-69+8138T>A
XM_011520411.1:c.-114+8138T>A XP_011518713.1:n.-114+8138T>A
XM_011520411.3:c.-114+8138T>A XP_011518713.1:n.-114+8138T>A
XM_017018434.2:c.-114+8138T>A XP_016873923.1:n.-114+8138T>A
XM_017018435.2:c.-69+8138T>A XP_016873924.1:n.-69+8138T>A
XM_017018436.1:c.-53+8138T>A XP_016873925.1:n.-53+8138T>A
XM_017018437.1:c.-114+8138T>A XP_016873926.1:n.-114+8138T>A
XM_017018439.1:c.-53+8138T>A XP_016873928.1:n.-53+8138T>A
XM_017018440.2:c.-114+8138T>A XP_016873929.1:n.-114+8138T>A
XM_017018441.2:c.-114+8138T>A XP_016873930.1:n.-114+8138T>A
NM_006906.2:c.-114+8138T>A MANE Select NP_008837.1:n.-114+8138T>A
NM_001039970.2:c.-114+8138T>A NP_001035059.1:n.-114+8138T>A
NM_001278238.2:c.-53+8138T>A NP_001265167.1:n.-53+8138T>A
NM_001278239.2:c.-53+8138T>A NP_001265168.1:n.-53+8138T>A
NM_032781.4:c.-69+8138T>A NP_116170.3:n.-69+8138T>A