Canonical Allele Identifier: CA2620022628

Gene: PTPRQ

Linked Data

• gnomAD v4: 12-80460724-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460724G>T , CM000674.2:g.80460724G>T	GRCh38
NC_000012.11:g.80849453C>A , CM000674.1:g.80849453C>A	GRCh37
NC_000012.10:g.79373584C>A	NCBI36
NG_034052.1:g.21379G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.732G>T MANE Select	ENSP00000495607.1:p.Ser244=
ENST00000614701.4:c.732G>T	ENSP00000482885.1:p.Ser244=
ENST00000616559.4:c.858G>T	ENSP00000483259.1:p.Ser286=
NM_001145026.1:c.732G>T	NP_001138498.1:p.Ser244=
XM_011538290.1:c.732G>T	XP_011536592.1:p.Ser244=
XM_017019273.1:c.1398G>T	XP_016874762.1:p.Ser466=
XM_017019274.1:c.1398G>T	XP_016874763.1:p.Ser466=
XM_017019275.1:c.1398G>T	XP_016874764.1:p.Ser466=
XR_001748688.1:n.1535G>T
XR_001748689.1:n.1535G>T
NM_001145026.2:c.732G>T MANE Select	NP_001138498.1:p.Ser244=