Canonical Allele Identifier: CA385875524

Gene: PTPRQ

Linked Data

• dbSNP Id: rs1282735378
• gnomAD v3: 12-80460654-A-G
• gnomAD v4: 12-80460654-A-G
• MyVariant Identifiers: chr12:g.80849523T>C (hg19) ; chr12:g.80460654A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460654A>G , CM000674.2:g.80460654A>G	GRCh38
NC_000012.11:g.80849523T>C , CM000674.1:g.80849523T>C	GRCh37
NC_000012.10:g.79373654T>C	NCBI36
NG_034052.1:g.21309A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.662A>G MANE Select	ENSP00000495607.1:p.Glu221Gly
ENST00000614701.4:c.662A>G	ENSP00000482885.1:p.Glu221Gly
ENST00000616559.4:c.788A>G	ENSP00000483259.1:p.Glu263Gly
NM_001145026.1:c.662A>G	NP_001138498.1:p.Glu221Gly
XM_011538290.1:c.662A>G	XP_011536592.1:p.Glu221Gly
XM_017019273.1:c.1328A>G	XP_016874762.1:p.Glu443Gly
XM_017019274.1:c.1328A>G	XP_016874763.1:p.Glu443Gly
XM_017019275.1:c.1328A>G	XP_016874764.1:p.Glu443Gly
XR_001748688.1:n.1465A>G
XR_001748689.1:n.1465A>G
NM_001145026.2:c.662A>G MANE Select	NP_001138498.1:p.Glu221Gly