Canonical Allele Identifier: CA385875618

Gene: PTPRQ

Linked Data

• gnomAD v4: 12-80460662-G-A
• MyVariant Identifiers: chr12:g.80460662G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460662G>A , CM000674.2:g.80460662G>A	GRCh38
NC_000012.11:g.80849515C>T , CM000674.1:g.80849515C>T	GRCh37
NC_000012.10:g.79373646C>T	NCBI36
NG_034052.1:g.21317G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.670G>A MANE Select	ENSP00000495607.1:p.Glu224Lys
ENST00000614701.4:c.670G>A	ENSP00000482885.1:p.Glu224Lys
ENST00000616559.4:c.796G>A	ENSP00000483259.1:p.Glu266Lys
NM_001145026.1:c.670G>A	NP_001138498.1:p.Glu224Lys
XM_011538290.1:c.670G>A	XP_011536592.1:p.Glu224Lys
XM_017019273.1:c.1336G>A	XP_016874762.1:p.Glu446Lys
XM_017019274.1:c.1336G>A	XP_016874763.1:p.Glu446Lys
XM_017019275.1:c.1336G>A	XP_016874764.1:p.Glu446Lys
XR_001748688.1:n.1473G>A
XR_001748689.1:n.1473G>A
NM_001145026.2:c.670G>A MANE Select	NP_001138498.1:p.Glu224Lys