Canonical Allele Identifier: CA233449306

Gene: PTPRO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.15358728A>G , CM000674.2:g.15358728A>G	GRCh38
NC_000012.11:g.15511662A>G , CM000674.1:g.15511662A>G	GRCh37
NC_000012.10:g.15402929A>G	NCBI36
NG_031857.1:g.41472A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_030667.3:c.75+35927A>G MANE Select	NP_109592.1:n.75+35927A>G
ENST00000281171.9:c.75+35927A>G MANE Select	ENSP00000281171.4:n.75+35927A>G
NM_002848.3:c.75+35927A>G	NP_002839.1:n.75+35927A>G
NM_002848.4:c.75+35927A>G	NP_002839.1:n.75+35927A>G
NM_030667.2:c.75+35927A>G	NP_109592.1:n.75+35927A>G
ENST00000281171.8:c.75+35927A>G	ENSP00000281171.4:n.75+35927A>G
ENST00000348962.6:c.75+35927A>G	ENSP00000343434.2:n.75+35927A>G
ENST00000348962.7:c.75+35927A>G	ENSP00000343434.2:n.75+35927A>G
ENST00000543886.5:c.75+35927A>G	ENSP00000444173.1:n.75+35927A>G
ENST00000543886.6:c.75+35927A>G	ENSP00000444173.1:n.75+35927A>G
ENST00000545023.1:n.25+35927A>G
ENST00000674186.1:n.375+35927A>G
ENST00000674188.1:c.75+35927A>G	ENSP00000501325.1:n.75+35927A>G
ENST00000674261.1:c.75+35927A>G	ENSP00000501538.1:n.75+35927A>G
ENST00000674286.1:c.-421+35650A>G	ENSP00000501361.1:n.-421+35650A>G
ENST00000674316.1:c.75+35927A>G	ENSP00000501352.1:n.75+35927A>G
ENST00000674391.1:c.75+35927A>G	ENSP00000501451.1:n.75+35927A>G
ENST00000674483.1:n.420A>G
XM_011520792.1:c.75+35927A>G	XP_011519094.1:n.75+35927A>G
XM_017019725.2:c.75+35927A>G	XP_016875214.1:n.75+35927A>G
XR_931316.1:n.468+35927A>G
XR_931316.3:n.468+35927A>G