Canonical Allele Identifier: CA6466623

Gene: PTPRO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.15520169C>T , CM000674.2:g.15520169C>T	GRCh38
NC_000012.11:g.15673103C>T , CM000674.1:g.15673103C>T	GRCh37
NC_000012.10:g.15564370C>T	NCBI36
NG_031857.1:g.202913C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_030667.3:c.1780-32C>T MANE Select	NP_109592.1:n.1780-32C>T
ENST00000281171.9:c.1780-32C>T MANE Select	ENSP00000281171.4:n.1780-32C>T
NM_002848.3:c.1780-32C>T	NP_002839.1:n.1780-32C>T
NM_002848.4:c.1780-32C>T	NP_002839.1:n.1780-32C>T
NM_030667.2:c.1780-32C>T	NP_109592.1:n.1780-32C>T
ENST00000281171.8:c.1780-32C>T	ENSP00000281171.4:n.1780-32C>T
ENST00000348962.6:c.1780-32C>T	ENSP00000343434.2:n.1780-32C>T
ENST00000348962.7:c.1780-32C>T	ENSP00000343434.2:n.1780-32C>T
ENST00000674188.1:c.1336-32C>T	ENSP00000501325.1:n.1336-32C>T
ENST00000674261.1:c.1780-32C>T	ENSP00000501538.1:n.1780-32C>T
ENST00000674286.1:c.1285-32C>T	ENSP00000501361.1:n.1285-32C>T
ENST00000674316.1:c.1780-32C>T	ENSP00000501352.1:n.1780-32C>T
ENST00000674391.1:c.*1242-32C>T	ENSP00000501451.1:n.*1242-32C>T
XM_011520792.1:c.1336-32C>T	XP_011519094.1:n.1336-32C>T
XM_017019725.2:c.1780-32C>T	XP_016875214.1:n.1780-32C>T
XR_931316.1:n.2173-32C>T
XR_931316.3:n.2173-32C>T