Canonical Allele Identifier: CA385876061

Gene: PTPRQ

Linked Data

• MyVariant Identifiers: chr12:g.80460705G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460705G>T , CM000674.2:g.80460705G>T	GRCh38
NC_000012.11:g.80849472C>A , CM000674.1:g.80849472C>A	GRCh37
NC_000012.10:g.79373603C>A	NCBI36
NG_034052.1:g.21360G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.713G>T MANE Select	ENSP00000495607.1:p.Gly238Val
ENST00000614701.4:c.713G>T	ENSP00000482885.1:p.Gly238Val
ENST00000616559.4:c.839G>T	ENSP00000483259.1:p.Gly280Val
NM_001145026.1:c.713G>T	NP_001138498.1:p.Gly238Val
XM_011538290.1:c.713G>T	XP_011536592.1:p.Gly238Val
XM_017019273.1:c.1379G>T	XP_016874762.1:p.Gly460Val
XM_017019274.1:c.1379G>T	XP_016874763.1:p.Gly460Val
XM_017019275.1:c.1379G>T	XP_016874764.1:p.Gly460Val
XR_001748688.1:n.1516G>T
XR_001748689.1:n.1516G>T
NM_001145026.2:c.713G>T MANE Select	NP_001138498.1:p.Gly238Val