Canonical Allele Identifier: CA385883522

Gene: PTPRQ

Linked Data

• MyVariant Identifiers: chr12:g.80878227T>A (hg19) ; chr12:g.80484448T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484448T>A , CM000674.2:g.80484448T>A	GRCh38
NC_000012.11:g.80878227T>A , CM000674.1:g.80878227T>A	GRCh37
NC_000012.10:g.79402358T>A	NCBI36
NG_034052.1:g.45103T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1202T>A MANE Select	ENSP00000495607.1:p.Phe401Tyr
ENST00000614701.4:c.1202T>A	ENSP00000482885.1:p.Phe401Tyr
ENST00000616559.4:c.1328T>A	ENSP00000483259.1:p.Phe443Tyr
NM_001145026.1:c.1202T>A	NP_001138498.1:p.Phe401Tyr
XM_011538290.1:c.1202T>A	XP_011536592.1:p.Phe401Tyr
XM_017019273.1:c.1868T>A	XP_016874762.1:p.Phe623Tyr
XM_017019274.1:c.1868T>A	XP_016874763.1:p.Phe623Tyr
XM_017019275.1:c.1868T>A	XP_016874764.1:p.Phe623Tyr
XR_001748688.1:n.2005T>A
XR_001748689.1:n.2005T>A
NM_001145026.2:c.1202T>A MANE Select	NP_001138498.1:p.Phe401Tyr