Canonical Allele Identifier: CA2049296173

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80539915A= , CM000674.2:g.80539915A=	GRCh38
NC_000012.11:g.80933694A= , CM000674.1:g.80933694A=	GRCh37
NC_000012.10:g.79457825A=	NCBI36
NG_034052.1:g.100570A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001145026.2:c.3125A= MANE Select	NP_001138498.1:p.Asp1042=
ENST00000644991.3:c.3125A= MANE Select	ENSP00000495607.1:p.Asp1042=
NM_001145026.1:c.3125A=	NP_001138498.1:p.Asp1042=
ENST00000614701.4:c.3125A=	ENSP00000482885.1:p.Asp1042=
ENST00000616559.4:c.3251A=	ENSP00000483259.1:p.Asp1084=
XM_011538290.1:c.3125A=	XP_011536592.1:p.Asp1042=
XM_017019273.1:c.3791A=	XP_016874762.1:p.Asp1264=
XM_017019274.1:c.3791A=	XP_016874763.1:p.Asp1264=
XM_017019275.1:c.3791A=	XP_016874764.1:p.Asp1264=
XR_001748688.1:n.3928A=
XR_001748689.1:n.3928A=