Canonical Allele Identifier: CA6466572

Gene: PTPRO

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.15516803T>C , CM000674.2:g.15516803T>C	GRCh38
NC_000012.11:g.15669737T>C , CM000674.1:g.15669737T>C	GRCh37
NC_000012.10:g.15561004T>C	NCBI36
NG_031857.1:g.199547T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_030667.3:c.1626T>C MANE Select	NP_109592.1:p.Gly542=
ENST00000281171.9:c.1626T>C MANE Select	ENSP00000281171.4:p.Gly542=
NM_002848.3:c.1626T>C	NP_002839.1:p.Gly542=
NM_002848.4:c.1626T>C	NP_002839.1:p.Gly542=
NM_030667.2:c.1626T>C	NP_109592.1:p.Gly542=
ENST00000281171.8:c.1626T>C	ENSP00000281171.4:p.Gly542=
ENST00000348962.6:c.1626T>C	ENSP00000343434.2:p.Gly542=
ENST00000348962.7:c.1626T>C	ENSP00000343434.2:p.Gly542=
ENST00000543886.5:c.1626T>C	ENSP00000444173.1:p.Gly542=
ENST00000543886.6:c.1626T>C	ENSP00000444173.1:p.Gly542=
ENST00000674188.1:c.1182T>C	ENSP00000501325.1:p.Gly394=
ENST00000674261.1:c.1626T>C	ENSP00000501538.1:p.Gly542=
ENST00000674286.1:c.1131T>C	ENSP00000501361.1:p.Gly377=
ENST00000674316.1:c.1626T>C	ENSP00000501352.1:p.Gly542=
ENST00000674391.1:c.*1088T>C	ENSP00000501451.1:n.*1088T>C
XM_011520792.1:c.1182T>C	XP_011519094.1:p.Gly394=
XM_017019725.2:c.1626T>C	XP_016875214.1:p.Gly542=
XR_931316.1:n.2019T>C
XR_931316.3:n.2019T>C