Canonical Allele Identifier: CA2049270691

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484441G= , CM000674.2:g.80484441G=	GRCh38
NC_000012.11:g.80878220G= , CM000674.1:g.80878220G=	GRCh37
NC_000012.10:g.79402351G=	NCBI36
NG_034052.1:g.45096G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000644991.3:c.1195G= MANE Select	ENSP00000495607.1:p.Ala399=
ENST00000614701.4:c.1195G=	ENSP00000482885.1:p.Ala399=
ENST00000616559.4:c.1321G=	ENSP00000483259.1:p.Ala441=
NM_001145026.1:c.1195G=	NP_001138498.1:p.Ala399=
XM_011538290.1:c.1195G=	XP_011536592.1:p.Ala399=
XM_017019273.1:c.1861G=	XP_016874762.1:p.Ala621=
XM_017019274.1:c.1861G=	XP_016874763.1:p.Ala621=
XM_017019275.1:c.1861G=	XP_016874764.1:p.Ala621=
XR_001748688.1:n.1998G=
XR_001748689.1:n.1998G=
NM_001145026.2:c.1195G= MANE Select	NP_001138498.1:p.Ala399=