Canonical Allele Identifier: CA2620023766

Gene: PTPRQ

Linked Data

• gnomAD v4: 12-80484673-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484673G>T , CM000674.2:g.80484673G>T	GRCh38
NC_000012.11:g.80878452G>T , CM000674.1:g.80878452G>T	GRCh37
NC_000012.10:g.79402583G>T	NCBI36
NG_034052.1:g.45328G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1359+68G>T MANE Select	ENSP00000495607.1:n.1359+68G>T
ENST00000614701.4:c.1359+68G>T	ENSP00000482885.1:n.1359+68G>T
ENST00000616559.4:c.1485+68G>T	ENSP00000483259.1:n.1485+68G>T
NM_001145026.1:c.1359+68G>T	NP_001138498.1:n.1359+68G>T
XM_011538290.1:c.1359+68G>T	XP_011536592.1:n.1359+68G>T
XM_017019273.1:c.2025+68G>T	XP_016874762.1:n.2025+68G>T
XM_017019274.1:c.2025+68G>T	XP_016874763.1:n.2025+68G>T
XM_017019275.1:c.2025+68G>T	XP_016874764.1:n.2025+68G>T
XR_001748688.1:n.2162+68G>T
XR_001748689.1:n.2162+68G>T
NM_001145026.2:c.1359+68G>T MANE Select	NP_001138498.1:n.1359+68G>T