Canonical Allele Identifier: CA2049256786

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460654A= , CM000674.2:g.80460654A=	GRCh38
NC_000012.11:g.80849523T= , CM000674.1:g.80849523T=	GRCh37
NC_000012.10:g.79373654T=	NCBI36
NG_034052.1:g.21309A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.662A= MANE Select	ENSP00000495607.1:p.Glu221=
ENST00000614701.4:c.662A=	ENSP00000482885.1:p.Glu221=
ENST00000616559.4:c.788A=	ENSP00000483259.1:p.Glu263=
NM_001145026.1:c.662A=	NP_001138498.1:p.Glu221=
XM_011538290.1:c.662A=	XP_011536592.1:p.Glu221=
XM_017019273.1:c.1328A=	XP_016874762.1:p.Glu443=
XM_017019274.1:c.1328A=	XP_016874763.1:p.Glu443=
XM_017019275.1:c.1328A=	XP_016874764.1:p.Glu443=
XR_001748688.1:n.1465A=
XR_001748689.1:n.1465A=
NM_001145026.2:c.662A= MANE Select	NP_001138498.1:p.Glu221=