Canonical Allele Identifier: CA385876188

Gene: PTPRQ

Linked Data

• MyVariant Identifiers: chr12:g.80460732C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460732C>G , CM000674.2:g.80460732C>G	GRCh38
NC_000012.11:g.80849445G>C , CM000674.1:g.80849445G>C	GRCh37
NC_000012.10:g.79373576G>C	NCBI36
NG_034052.1:g.21387C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.740C>G MANE Select	ENSP00000495607.1:p.Thr247Arg
ENST00000614701.4:c.740C>G	ENSP00000482885.1:p.Thr247Arg
ENST00000616559.4:c.866C>G	ENSP00000483259.1:p.Thr289Arg
NM_001145026.1:c.740C>G	NP_001138498.1:p.Thr247Arg
XM_011538290.1:c.740C>G	XP_011536592.1:p.Thr247Arg
XM_017019273.1:c.1406C>G	XP_016874762.1:p.Thr469Arg
XM_017019274.1:c.1406C>G	XP_016874763.1:p.Thr469Arg
XM_017019275.1:c.1406C>G	XP_016874764.1:p.Thr469Arg
XR_001748688.1:n.1543C>G
XR_001748689.1:n.1543C>G
NM_001145026.2:c.740C>G MANE Select	NP_001138498.1:p.Thr247Arg