Canonical Allele Identifier: CA2049256860

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460839G= , CM000674.2:g.80460839G=	GRCh38
NC_000012.11:g.80849338C= , CM000674.1:g.80849338C=	GRCh37
NC_000012.10:g.79373469C=	NCBI36
NG_034052.1:g.21494G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644991.3:c.847G= MANE Select	ENSP00000495607.1:p.Val283=
ENST00000614701.4:c.847G=	ENSP00000482885.1:p.Val283=
ENST00000616559.4:c.973G=	ENSP00000483259.1:p.Val325=
NM_001145026.1:c.847G=	NP_001138498.1:p.Val283=
XM_011538290.1:c.847G=	XP_011536592.1:p.Val283=
XM_017019273.1:c.1513G=	XP_016874762.1:p.Val505=
XM_017019274.1:c.1513G=	XP_016874763.1:p.Val505=
XM_017019275.1:c.1513G=	XP_016874764.1:p.Val505=
XR_001748688.1:n.1650G=
XR_001748689.1:n.1650G=
NM_001145026.2:c.847G= MANE Select	NP_001138498.1:p.Val283=