Canonical Allele Identifier: CA6702404
Gene: PTPRQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80484479G>A , CM000674.2:g.80484479G>A GRCh38
NC_000012.11:g.80878258G>A , CM000674.1:g.80878258G>A GRCh37
NC_000012.10:g.79402389G>A NCBI36
NG_034052.1:g.45134G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001145026.2:c.1233G>A MANE Select NP_001138498.1:p.Thr411=
ENST00000644991.3:c.1233G>A MANE Select ENSP00000495607.1:p.Thr411=
NM_001145026.1:c.1233G>A NP_001138498.1:p.Thr411=
ENST00000614701.4:c.1233G>A ENSP00000482885.1:p.Thr411=
ENST00000616559.4:c.1359G>A ENSP00000483259.1:p.Thr453=
XM_011538290.1:c.1233G>A XP_011536592.1:p.Thr411=
XM_017019273.1:c.1899G>A XP_016874762.1:p.Thr633=
XM_017019274.1:c.1899G>A XP_016874763.1:p.Thr633=
XM_017019275.1:c.1899G>A XP_016874764.1:p.Thr633=
XR_001748688.1:n.2036G>A
XR_001748689.1:n.2036G>A