Canonical Allele Identifier: CA2620022632

Gene: PTPRQ

Linked Data

• gnomAD v4: 12-80460765-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460766del , CM000674.2:g.80460766del	GRCh38
NC_000012.11:g.80849411del , CM000674.1:g.80849411del	GRCh37
NC_000012.10:g.79373542del	NCBI36
NG_034052.1:g.21421del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.774del MANE Select	ENSP00000495607.1:p.Ser259AlafsTer11
ENST00000614701.4:c.774del	ENSP00000482885.1:p.Ser259AlafsTer11
ENST00000616559.4:c.900del	ENSP00000483259.1:p.Ser301AlafsTer11
NM_001145026.1:c.774del	NP_001138498.1:p.Ser259AlafsTer11
XM_011538290.1:c.774del	XP_011536592.1:p.Ser259AlafsTer11
XM_017019273.1:c.1440del	XP_016874762.1:p.Ser481AlafsTer11
XM_017019274.1:c.1440del	XP_016874763.1:p.Ser481AlafsTer11
XM_017019275.1:c.1440del	XP_016874764.1:p.Ser481AlafsTer11
XR_001748688.1:n.1577del
XR_001748689.1:n.1577del
NM_001145026.2:c.774del MANE Select	NP_001138498.1:p.Ser259AlafsTer11