Canonical Allele Identifier: CA2049333538

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80620153G= , CM000674.2:g.80620153G=	GRCh38
NC_000012.11:g.81013932G= , CM000674.1:g.81013932G=	GRCh37
NC_000012.10:g.79538063G=	NCBI36
NG_034052.1:g.180808G=

Transcript Alleles

HGVS	Amino-acid Change
NM_001145026.2:c.5390-1G= MANE Select	NP_001138498.1:n.5390-1G=
ENST00000644991.3:c.5390-1G= MANE Select	ENSP00000495607.1:n.5390-1G=
NM_001145026.1:c.5390-1G=	NP_001138498.1:n.5390-1G=
ENST00000614701.4:c.5390-1G=	ENSP00000482885.1:n.5390-1G=
ENST00000616559.4:c.5516-1G=	ENSP00000483259.1:n.5516-1G=
XM_011538290.1:c.5390-1G=	XP_011536592.1:n.5390-1G=
XM_017019273.1:c.6056-1G=	XP_016874762.1:n.6056-1G=
XM_017019274.1:c.6056-1G=	XP_016874763.1:n.6056-1G=
XM_017019275.1:c.6056-1G=	XP_016874764.1:n.6056-1G=
XR_001748688.1:n.6193-1G=
XR_001748689.1:n.6193-1G=
XR_001749222.1:n.121-39744C=