Canonical Allele Identifier: CA2796696872

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460708_80460713del , CM000674.2:g.80460708_80460713del	GRCh38
NC_000012.11:g.80849466_80849471del , CM000674.1:g.80849466_80849471del	GRCh37
NC_000012.10:g.79373597_79373602del	NCBI36
NG_034052.1:g.21363_21368del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.716_721del MANE Select	ENSP00000495607.1:p.Arg239_Val240del
ENST00000614701.4:c.716_721del	ENSP00000482885.1:p.Arg239_Val240del
ENST00000616559.4:c.842_847del	ENSP00000483259.1:p.Arg281_Val282del
NM_001145026.1:c.716_721del	NP_001138498.1:p.Arg239_Val240del
XM_011538290.1:c.716_721del	XP_011536592.1:p.Arg239_Val240del
XM_017019273.1:c.1382_1387del	XP_016874762.1:p.Arg461_Val462del
XM_017019274.1:c.1382_1387del	XP_016874763.1:p.Arg461_Val462del
XM_017019275.1:c.1382_1387del	XP_016874764.1:p.Arg461_Val462del
XR_001748688.1:n.1519_1524del
XR_001748689.1:n.1519_1524del
NM_001145026.2:c.716_721del MANE Select	NP_001138498.1:p.Arg239_Val240del