Canonical Allele Identifier: CA2049256788

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460659A= , CM000674.2:g.80460659A=	GRCh38
NC_000012.11:g.80849518T= , CM000674.1:g.80849518T=	GRCh37
NC_000012.10:g.79373649T=	NCBI36
NG_034052.1:g.21314A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.667A= MANE Select	ENSP00000495607.1:p.Ser223=
ENST00000614701.4:c.667A=	ENSP00000482885.1:p.Ser223=
ENST00000616559.4:c.793A=	ENSP00000483259.1:p.Ser265=
NM_001145026.1:c.667A=	NP_001138498.1:p.Ser223=
XM_011538290.1:c.667A=	XP_011536592.1:p.Ser223=
XM_017019273.1:c.1333A=	XP_016874762.1:p.Ser445=
XM_017019274.1:c.1333A=	XP_016874763.1:p.Ser445=
XM_017019275.1:c.1333A=	XP_016874764.1:p.Ser445=
XR_001748688.1:n.1470A=
XR_001748689.1:n.1470A=
NM_001145026.2:c.667A= MANE Select	NP_001138498.1:p.Ser223=