Canonical Allele Identifier: CA2049270725

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484531C= , CM000674.2:g.80484531C=	GRCh38
NC_000012.11:g.80878310C= , CM000674.1:g.80878310C=	GRCh37
NC_000012.10:g.79402441C=	NCBI36
NG_034052.1:g.45186C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001145026.2:c.1285C= MANE Select	NP_001138498.1:p.Gln429=
ENST00000644991.3:c.1285C= MANE Select	ENSP00000495607.1:p.Gln429=
NM_001145026.1:c.1285C=	NP_001138498.1:p.Gln429=
ENST00000614701.4:c.1285C=	ENSP00000482885.1:p.Gln429=
ENST00000616559.4:c.1411C=	ENSP00000483259.1:p.Gln471=
XM_011538290.1:c.1285C=	XP_011536592.1:p.Gln429=
XM_017019273.1:c.1951C=	XP_016874762.1:p.Gln651=
XM_017019274.1:c.1951C=	XP_016874763.1:p.Gln651=
XM_017019275.1:c.1951C=	XP_016874764.1:p.Gln651=
XR_001748688.1:n.2088C=
XR_001748689.1:n.2088C=