Canonical Allele Identifier: CA2620023748

Gene: PTPRQ

Linked Data

• gnomAD v4: 12-80484619-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484619A>G , CM000674.2:g.80484619A>G	GRCh38
NC_000012.11:g.80878398A>G , CM000674.1:g.80878398A>G	GRCh37
NC_000012.10:g.79402529A>G	NCBI36
NG_034052.1:g.45274A>G

Transcript Alleles

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