Canonical Allele Identifier: CA949699405

Gene: PTPRQ

Linked Data

• dbSNP Id: rs1894204790
• gnomAD v3: 12-80484436-CA-C
• gnomAD v4: 12-80484436-CA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484437del , CM000674.2:g.80484437del	GRCh38
NC_000012.11:g.80878216del , CM000674.1:g.80878216del	GRCh37
NC_000012.10:g.79402347del	NCBI36
NG_034052.1:g.45092del

Transcript Alleles

HGVS	Amino-acid change
ENST00000644991.3:c.1191del MANE Select	ENSP00000495607.1:p.Ala399GlnfsTer10
ENST00000614701.4:c.1191del	ENSP00000482885.1:p.Ala399GlnfsTer10
ENST00000616559.4:c.1317del	ENSP00000483259.1:p.Ala441GlnfsTer10
NM_001145026.1:c.1191del	NP_001138498.1:p.Ala399GlnfsTer10
XM_011538290.1:c.1191del	XP_011536592.1:p.Ala399GlnfsTer10
XM_017019273.1:c.1857del	XP_016874762.1:p.Ala621GlnfsTer10
XM_017019274.1:c.1857del	XP_016874763.1:p.Ala621GlnfsTer10
XM_017019275.1:c.1857del	XP_016874764.1:p.Ala621GlnfsTer10
XR_001748688.1:n.1994del
XR_001748689.1:n.1994del
NM_001145026.2:c.1191del MANE Select	NP_001138498.1:p.Ala399GlnfsTer10