Canonical Allele Identifier: CA2049270771

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484634G= , CM000674.2:g.80484634G=	GRCh38
NC_000012.11:g.80878413G= , CM000674.1:g.80878413G=	GRCh37
NC_000012.10:g.79402544G=	NCBI36
NG_034052.1:g.45289G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1359+29G= MANE Select	ENSP00000495607.1:n.1359+29G=
ENST00000614701.4:c.1359+29G=	ENSP00000482885.1:n.1359+29G=
ENST00000616559.4:c.1485+29G=	ENSP00000483259.1:n.1485+29G=
NM_001145026.1:c.1359+29G=	NP_001138498.1:n.1359+29G=
XM_011538290.1:c.1359+29G=	XP_011536592.1:n.1359+29G=
XM_017019273.1:c.2025+29G=	XP_016874762.1:n.2025+29G=
XM_017019274.1:c.2025+29G=	XP_016874763.1:n.2025+29G=
XM_017019275.1:c.2025+29G=	XP_016874764.1:n.2025+29G=
XR_001748688.1:n.2162+29G=
XR_001748689.1:n.2162+29G=
NM_001145026.2:c.1359+29G= MANE Select	NP_001138498.1:n.1359+29G=