Canonical Allele Identifier: CA2049270813

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484714_80484715delinsAG , CM000674.2:g.80484714_80484715delinsAG	GRCh38
NC_000012.11:g.80878493_80878494delinsAG , CM000674.1:g.80878493_80878494delinsAG	GRCh37
NC_000012.10:g.79402624_79402625delinsAG	NCBI36
NG_034052.1:g.45369_45370delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1359+109_1359+110delinsAG MANE Select	ENSP00000495607.1:n.1359+109_1359+110delinsAG
ENST00000614701.4:c.1359+109_1359+110delinsAG	ENSP00000482885.1:n.1359+109_1359+110delinsAG
ENST00000616559.4:c.1485+109_1485+110delinsAG	ENSP00000483259.1:n.1485+109_1485+110delinsAG
NM_001145026.1:c.1359+109_1359+110delinsAG	NP_001138498.1:n.1359+109_1359+110delinsAG
XM_011538290.1:c.1359+109_1359+110delinsAG	XP_011536592.1:n.1359+109_1359+110delinsAG
XM_017019273.1:c.2025+109_2025+110delinsAG	XP_016874762.1:n.2025+109_2025+110delinsAG
XM_017019274.1:c.2025+109_2025+110delinsAG	XP_016874763.1:n.2025+109_2025+110delinsAG
XM_017019275.1:c.2025+109_2025+110delinsAG	XP_016874764.1:n.2025+109_2025+110delinsAG
XR_001748688.1:n.2162+109_2162+110delinsAG
XR_001748689.1:n.2162+109_2162+110delinsAG
NM_001145026.2:c.1359+109_1359+110delinsAG MANE Select	NP_001138498.1:n.1359+109_1359+110delinsAG