Canonical Allele Identifier: CA385876846

Gene: PTPRQ

Linked Data

• MyVariant Identifiers: chr12:g.80460819A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460819A>T , CM000674.2:g.80460819A>T	GRCh38
NC_000012.11:g.80849358T>A , CM000674.1:g.80849358T>A	GRCh37
NC_000012.10:g.79373489T>A	NCBI36
NG_034052.1:g.21474A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.827A>T MANE Select	ENSP00000495607.1:p.Tyr276Phe
ENST00000614701.4:c.827A>T	ENSP00000482885.1:p.Tyr276Phe
ENST00000616559.4:c.953A>T	ENSP00000483259.1:p.Tyr318Phe
NM_001145026.1:c.827A>T	NP_001138498.1:p.Tyr276Phe
XM_011538290.1:c.827A>T	XP_011536592.1:p.Tyr276Phe
XM_017019273.1:c.1493A>T	XP_016874762.1:p.Tyr498Phe
XM_017019274.1:c.1493A>T	XP_016874763.1:p.Tyr498Phe
XM_017019275.1:c.1493A>T	XP_016874764.1:p.Tyr498Phe
XR_001748688.1:n.1630A>T
XR_001748689.1:n.1630A>T
NM_001145026.2:c.827A>T MANE Select	NP_001138498.1:p.Tyr276Phe