Canonical Allele Identifier: CA2049256805

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460699C= , CM000674.2:g.80460699C=	GRCh38
NC_000012.11:g.80849478G= , CM000674.1:g.80849478G=	GRCh37
NC_000012.10:g.79373609G=	NCBI36
NG_034052.1:g.21354C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.707C= MANE Select	ENSP00000495607.1:p.Thr236=
ENST00000614701.4:c.707C=	ENSP00000482885.1:p.Thr236=
ENST00000616559.4:c.833C=	ENSP00000483259.1:p.Thr278=
NM_001145026.1:c.707C=	NP_001138498.1:p.Thr236=
XM_011538290.1:c.707C=	XP_011536592.1:p.Thr236=
XM_017019273.1:c.1373C=	XP_016874762.1:p.Thr458=
XM_017019274.1:c.1373C=	XP_016874763.1:p.Thr458=
XM_017019275.1:c.1373C=	XP_016874764.1:p.Thr458=
XR_001748688.1:n.1510C=
XR_001748689.1:n.1510C=
NM_001145026.2:c.707C= MANE Select	NP_001138498.1:p.Thr236=