Canonical Allele Identifier: CA2049256812

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460715A= , CM000674.2:g.80460715A=	GRCh38
NC_000012.11:g.80849462T= , CM000674.1:g.80849462T=	GRCh37
NC_000012.10:g.79373593T=	NCBI36
NG_034052.1:g.21370A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.723A= MANE Select	ENSP00000495607.1:p.Thr241=
ENST00000614701.4:c.723A=	ENSP00000482885.1:p.Thr241=
ENST00000616559.4:c.849A=	ENSP00000483259.1:p.Thr283=
NM_001145026.1:c.723A=	NP_001138498.1:p.Thr241=
XM_011538290.1:c.723A=	XP_011536592.1:p.Thr241=
XM_017019273.1:c.1389A=	XP_016874762.1:p.Thr463=
XM_017019274.1:c.1389A=	XP_016874763.1:p.Thr463=
XM_017019275.1:c.1389A=	XP_016874764.1:p.Thr463=
XR_001748688.1:n.1526A=
XR_001748689.1:n.1526A=
NM_001145026.2:c.723A= MANE Select	NP_001138498.1:p.Thr241=