Canonical Allele Identifier: CA2049256799

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460684C= , CM000674.2:g.80460684C=	GRCh38
NC_000012.11:g.80849493G= , CM000674.1:g.80849493G=	GRCh37
NC_000012.10:g.79373624G=	NCBI36
NG_034052.1:g.21339C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.692C= MANE Select	ENSP00000495607.1:p.Ala231=
ENST00000614701.4:c.692C=	ENSP00000482885.1:p.Ala231=
ENST00000616559.4:c.818C=	ENSP00000483259.1:p.Ala273=
NM_001145026.1:c.692C=	NP_001138498.1:p.Ala231=
XM_011538290.1:c.692C=	XP_011536592.1:p.Ala231=
XM_017019273.1:c.1358C=	XP_016874762.1:p.Ala453=
XM_017019274.1:c.1358C=	XP_016874763.1:p.Ala453=
XM_017019275.1:c.1358C=	XP_016874764.1:p.Ala453=
XR_001748688.1:n.1495C=
XR_001748689.1:n.1495C=
NM_001145026.2:c.692C= MANE Select	NP_001138498.1:p.Ala231=