Canonical Allele Identifier: CA6466436
Gene: PTPRO HGNC NCBI
COSMIC:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.15503898T>A , CM000674.2:g.15503898T>A GRCh38
NC_000012.11:g.15656832T>A , CM000674.1:g.15656832T>A GRCh37
NC_000012.10:g.15548099T>A NCBI36
NG_031857.1:g.186642T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281171.9:c.1106-10T>A MANE Select ENSP00000281171.4:n.1106-10T>A
ENST00000348962.7:c.1106-10T>A ENSP00000343434.2:n.1106-10T>A
ENST00000543886.6:c.1106-10T>A ENSP00000444173.1:n.1106-10T>A
ENST00000674188.1:c.662-10T>A ENSP00000501325.1:n.662-10T>A
ENST00000674261.1:c.1106-10T>A ENSP00000501538.1:n.1106-10T>A
ENST00000674286.1:c.611-10T>A ENSP00000501361.1:n.611-10T>A
ENST00000674316.1:c.1106-10T>A ENSP00000501352.1:n.1106-10T>A
ENST00000674391.1:c.*558T>A ENSP00000501451.1:n.*558T>A
ENST00000281171.8:c.1106-10T>A ENSP00000281171.4:n.1106-10T>A
ENST00000348962.6:c.1106-10T>A ENSP00000343434.2:n.1106-10T>A
ENST00000543886.5:c.1106-10T>A ENSP00000444173.1:n.1106-10T>A
NM_002848.3:c.1106-10T>A NP_002839.1:n.1106-10T>A
NM_030667.2:c.1106-10T>A NP_109592.1:n.1106-10T>A
XM_011520792.1:c.662-10T>A XP_011519094.1:n.662-10T>A
XR_931316.1:n.1499-10T>A
XM_017019725.2:c.1106-10T>A XP_016875214.1:n.1106-10T>A
XR_931316.3:n.1499-10T>A
NM_030667.3:c.1106-10T>A MANE Select NP_109592.1:n.1106-10T>A
NM_002848.4:c.1106-10T>A NP_002839.1:n.1106-10T>A