Canonical Allele Identifier: CA2499306832
Gene: PTPRQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80460718_80460720del , CM000674.2:g.80460718_80460720del GRCh38
NC_000012.11:g.80849459_80849461del , CM000674.1:g.80849459_80849461del GRCh37
NC_000012.10:g.79373590_79373592del NCBI36
NG_034052.1:g.21373_21375del

Transcript Alleles

HGVS Amino-acid Change
ENST00000644991.3:c.726_728del MANE Select ENSP00000495607.1:p.Pro243del
ENST00000614701.4:c.726_728del ENSP00000482885.1:p.Pro243del
ENST00000616559.4:c.852_854del ENSP00000483259.1:p.Pro285del
NM_001145026.1:c.726_728del NP_001138498.1:p.Pro243del
XM_011538290.1:c.726_728del XP_011536592.1:p.Pro243del
XM_017019273.1:c.1392_1394del XP_016874762.1:p.Pro465del
XM_017019274.1:c.1392_1394del XP_016874763.1:p.Pro465del
XM_017019275.1:c.1392_1394del XP_016874764.1:p.Pro465del
XR_001748688.1:n.1529_1531del
XR_001748689.1:n.1529_1531del
NM_001145026.2:c.726_728del MANE Select NP_001138498.1:p.Pro243del