Canonical Allele Identifier: CA2049270763

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484619_80484620delinsAT , CM000674.2:g.80484619_80484620delinsAT	GRCh38
NC_000012.11:g.80878398_80878399delinsAT , CM000674.1:g.80878398_80878399delinsAT	GRCh37
NC_000012.10:g.79402529_79402530delinsAT	NCBI36
NG_034052.1:g.45274_45275delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1359+14_1359+15delinsAT MANE Select	ENSP00000495607.1:n.1359+14_1359+15delinsAT
ENST00000614701.4:c.1359+14_1359+15delinsAT	ENSP00000482885.1:n.1359+14_1359+15delinsAT
ENST00000616559.4:c.1485+14_1485+15delinsAT	ENSP00000483259.1:n.1485+14_1485+15delinsAT
NM_001145026.1:c.1359+14_1359+15delinsAT	NP_001138498.1:n.1359+14_1359+15delinsAT
XM_011538290.1:c.1359+14_1359+15delinsAT	XP_011536592.1:n.1359+14_1359+15delinsAT
XM_017019273.1:c.2025+14_2025+15delinsAT	XP_016874762.1:n.2025+14_2025+15delinsAT
XM_017019274.1:c.2025+14_2025+15delinsAT	XP_016874763.1:n.2025+14_2025+15delinsAT
XM_017019275.1:c.2025+14_2025+15delinsAT	XP_016874764.1:n.2025+14_2025+15delinsAT
XR_001748688.1:n.2162+14_2162+15delinsAT
XR_001748689.1:n.2162+14_2162+15delinsAT
NM_001145026.2:c.1359+14_1359+15delinsAT MANE Select	NP_001138498.1:n.1359+14_1359+15delinsAT