Canonical Allele Identifier: CA13734040
Gene: PTPRO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.15582508G>A , CM000674.2:g.15582508G>A GRCh38
NC_000012.11:g.15735442G>A , CM000674.1:g.15735442G>A GRCh37
NC_000012.10:g.15626709G>A NCBI36
NG_031857.1:g.265252G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000281171.9:c.3255+707G>A MANE Select ENSP00000281171.4:n.3255+707G>A
ENST00000348962.7:c.3171+707G>A ENSP00000343434.2:n.3171+707G>A
ENST00000442921.7:c.822+707G>A ENSP00000404188.2:n.822+707G>A
ENST00000544706.2:c.786+707G>A ENSP00000501413.1:n.786+707G>A
ENST00000674188.1:c.2811+707G>A ENSP00000501325.1:n.2811+707G>A
ENST00000674220.1:c.*419+707G>A ENSP00000501384.1:n.*419+707G>A
ENST00000674261.1:c.3255+707G>A ENSP00000501538.1:n.3255+707G>A
ENST00000674286.1:c.2760+707G>A ENSP00000501361.1:n.2760+707G>A
ENST00000674316.1:c.3255+707G>A ENSP00000501352.1:n.3255+707G>A
ENST00000674352.1:c.1075+707G>A
ENST00000674385.1:c.880+707G>A
ENST00000674388.1:c.822+707G>A ENSP00000501494.1:n.822+707G>A
ENST00000674391.1:c.*2717+707G>A ENSP00000501451.1:n.*2717+707G>A
ENST00000674434.1:n.2223+707G>A
ENST00000281171.8:c.3255+707G>A ENSP00000281171.4:n.3255+707G>A
ENST00000348962.6:c.3171+707G>A ENSP00000343434.2:n.3171+707G>A
ENST00000442921.6:c.822+707G>A ENSP00000404188.2:n.822+707G>A
ENST00000445537.6:c.822+707G>A ENSP00000393449.2:n.822+707G>A
ENST00000535322.1:c.192+707G>A ENSP00000446201.1:n.192+707G>A
ENST00000542557.5:c.738+707G>A ENSP00000437571.1:n.738+707G>A
ENST00000544244.5:c.738+707G>A ENSP00000439234.1:n.738+707G>A
NM_002848.3:c.3171+707G>A NP_002839.1:n.3171+707G>A
NM_030667.2:c.3255+707G>A NP_109592.1:n.3255+707G>A
NM_030668.2:c.738+707G>A NP_109593.1:n.738+707G>A
NM_030669.2:c.822+707G>A NP_109594.1:n.822+707G>A
NM_030670.2:c.738+707G>A NP_109595.1:n.738+707G>A
NM_030671.2:c.822+707G>A NP_109596.1:n.822+707G>A
XM_011520792.1:c.2811+707G>A XP_011519094.1:n.2811+707G>A
XR_931316.1:n.3648+707G>A
XR_931317.1:n.1309+707G>A
XR_931318.1:n.1225+707G>A
XR_931316.3:n.3648+707G>A
XR_931318.2:n.1220+707G>A
NM_030667.3:c.3255+707G>A MANE Select NP_109592.1:n.3255+707G>A
NM_002848.4:c.3171+707G>A NP_002839.1:n.3171+707G>A
NM_030668.3:c.738+707G>A NP_109593.1:n.738+707G>A
NM_030669.3:c.822+707G>A NP_109594.1:n.822+707G>A
NM_030670.3:c.738+707G>A NP_109595.1:n.738+707G>A
NM_030671.3:c.822+707G>A NP_109596.1:n.822+707G>A