Canonical Allele Identifier: CA2580086689
Community Standard Title: NM_001145026.2(PTPRQ):c.2726del (p.Glu909GlyfsTer15)
Gene: PTPRQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80534062del , CM000674.2:g.80534062del GRCh38
NC_000012.11:g.80927841del , CM000674.1:g.80927841del GRCh37
NC_000012.10:g.79451972del NCBI36
NG_034052.1:g.94717del

Transcript Alleles

HGVS Amino-acid Change
NM_001145026.2:c.2726del MANE Select NP_001138498.1:p.Glu909GlyfsTer15
ENST00000644991.3:c.2726del MANE Select ENSP00000495607.1:p.Glu909GlyfsTer15
NM_001145026.1:c.2726del NP_001138498.1:p.Glu909GlyfsTer15
ENST00000547485.1:n.282del
ENST00000614701.4:c.2726del ENSP00000482885.1:p.Glu909GlyfsTer15
ENST00000616559.4:c.2852del ENSP00000483259.1:p.Glu951GlyfsTer15
XM_011538290.1:c.2726del XP_011536592.1:p.Glu909GlyfsTer15
XM_017019273.1:c.3392del XP_016874762.1:p.Glu1131GlyfsTer15
XM_017019274.1:c.3392del XP_016874763.1:p.Glu1131GlyfsTer15
XM_017019275.1:c.3392del XP_016874764.1:p.Glu1131GlyfsTer15
XR_001748688.1:n.3529del
XR_001748689.1:n.3529del