Canonical Allele Identifier: CA2049256755

Gene: PTPRQ

Linked Data

• dbSNP Id: rs1893129600
• gnomAD v4: 12-80460604-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460606del , CM000674.2:g.80460606del	GRCh38
NC_000012.11:g.80849572del , CM000674.1:g.80849572del	GRCh37
NC_000012.10:g.79373703del	NCBI36
NG_034052.1:g.21261del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.661-47del MANE Select	ENSP00000495607.1:n.661-47del
ENST00000614701.4:c.661-47del	ENSP00000482885.1:n.661-47del
ENST00000616559.4:c.787-47del	ENSP00000483259.1:n.787-47del
NM_001145026.1:c.661-47del	NP_001138498.1:n.661-47del
XM_011538290.1:c.661-47del	XP_011536592.1:n.661-47del
XM_017019273.1:c.1327-47del	XP_016874762.1:n.1327-47del
XM_017019274.1:c.1327-47del	XP_016874763.1:n.1327-47del
XM_017019275.1:c.1327-47del	XP_016874764.1:n.1327-47del
XR_001748688.1:n.1464-47del
XR_001748689.1:n.1464-47del
NM_001145026.2:c.661-47del MANE Select	NP_001138498.1:n.661-47del