Canonical Allele Identifier: CA2049270805

Gene: PTPRQ

Linked Data

• dbSNP Id: rs1894215664

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484692_80484693del , CM000674.2:g.80484692_80484693del	GRCh38
NC_000012.11:g.80878471_80878472del , CM000674.1:g.80878471_80878472del	GRCh37
NC_000012.10:g.79402602_79402603del	NCBI36
NG_034052.1:g.45347_45348del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1359+87_1359+88del MANE Select	ENSP00000495607.1:n.1359+87_1359+88del
ENST00000614701.4:c.1359+87_1359+88del	ENSP00000482885.1:n.1359+87_1359+88del
ENST00000616559.4:c.1485+87_1485+88del	ENSP00000483259.1:n.1485+87_1485+88del
NM_001145026.1:c.1359+87_1359+88del	NP_001138498.1:n.1359+87_1359+88del
XM_011538290.1:c.1359+87_1359+88del	XP_011536592.1:n.1359+87_1359+88del
XM_017019273.1:c.2025+87_2025+88del	XP_016874762.1:n.2025+87_2025+88del
XM_017019274.1:c.2025+87_2025+88del	XP_016874763.1:n.2025+87_2025+88del
XM_017019275.1:c.2025+87_2025+88del	XP_016874764.1:n.2025+87_2025+88del
XR_001748688.1:n.2162+87_2162+88del
XR_001748689.1:n.2162+87_2162+88del
NM_001145026.2:c.1359+87_1359+88del MANE Select	NP_001138498.1:n.1359+87_1359+88del