Canonical Allele Identifier: CA6466281

Gene: PTPRO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.15497422G>A , CM000674.2:g.15497422G>A	GRCh38
NC_000012.11:g.15650356G>A , CM000674.1:g.15650356G>A	GRCh37
NC_000012.10:g.15541623G>A	NCBI36
NG_031857.1:g.180166G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000281171.9:c.508+19G>A MANE Select	ENSP00000281171.4:n.508+19G>A
ENST00000348962.7:c.508+19G>A	ENSP00000343434.2:n.508+19G>A
ENST00000543886.6:c.508+19G>A	ENSP00000444173.1:n.508+19G>A
ENST00000674188.1:c.508+19G>A	ENSP00000501325.1:n.508+19G>A
ENST00000674261.1:c.508+19G>A	ENSP00000501538.1:n.508+19G>A
ENST00000674286.1:c.13+19G>A	ENSP00000501361.1:n.13+19G>A
ENST00000674316.1:c.508+19G>A	ENSP00000501352.1:n.508+19G>A
ENST00000674391.1:c.508+19G>A	ENSP00000501451.1:n.508+19G>A
ENST00000281171.8:c.508+19G>A	ENSP00000281171.4:n.508+19G>A
ENST00000348962.6:c.508+19G>A	ENSP00000343434.2:n.508+19G>A
ENST00000543886.5:c.508+19G>A	ENSP00000444173.1:n.508+19G>A
NM_002848.3:c.508+19G>A	NP_002839.1:n.508+19G>A
NM_030667.2:c.508+19G>A	NP_109592.1:n.508+19G>A
XM_011520792.1:c.508+19G>A	XP_011519094.1:n.508+19G>A
XR_931316.1:n.901+19G>A
XM_017019725.2:c.508+19G>A	XP_016875214.1:n.508+19G>A
XR_931316.3:n.901+19G>A
NM_030667.3:c.508+19G>A MANE Select	NP_109592.1:n.508+19G>A
NM_002848.4:c.508+19G>A	NP_002839.1:n.508+19G>A