Canonical Allele Identifier: CA2796696599

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484764_80484765del , CM000674.2:g.80484764_80484765del	GRCh38
NC_000012.11:g.80878543_80878544del , CM000674.1:g.80878543_80878544del	GRCh37
NC_000012.10:g.79402674_79402675del	NCBI36
NG_034052.1:g.45419_45420del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1359+159_1359+160del MANE Select	ENSP00000495607.1:n.1359+159_1359+160del
ENST00000614701.4:c.1359+159_1359+160del	ENSP00000482885.1:n.1359+159_1359+160del
ENST00000616559.4:c.1485+159_1485+160del	ENSP00000483259.1:n.1485+159_1485+160del
NM_001145026.1:c.1359+159_1359+160del	NP_001138498.1:n.1359+159_1359+160del
XM_011538290.1:c.1359+159_1359+160del	XP_011536592.1:n.1359+159_1359+160del
XM_017019273.1:c.2025+159_2025+160del	XP_016874762.1:n.2025+159_2025+160del
XM_017019274.1:c.2025+159_2025+160del	XP_016874763.1:n.2025+159_2025+160del
XM_017019275.1:c.2025+159_2025+160del	XP_016874764.1:n.2025+159_2025+160del
XR_001748688.1:n.2162+159_2162+160del
XR_001748689.1:n.2162+159_2162+160del
NM_001145026.2:c.1359+159_1359+160del MANE Select	NP_001138498.1:n.1359+159_1359+160del