Canonical Allele Identifier: CA6702807
Community Standard Title: NM_001145026.2(PTPRQ):c.5196A>C (p.Pro1732=)
Gene: PTPRQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80616232A>C , CM000674.2:g.80616232A>C GRCh38
NC_000012.11:g.81010011A>C , CM000674.1:g.81010011A>C GRCh37
NC_000012.10:g.79534142A>C NCBI36
NG_034052.1:g.176887A>C

Transcript Alleles

HGVS Amino-acid Change
NM_001145026.2:c.5196A>C MANE Select NP_001138498.1:p.Pro1732=
ENST00000644991.3:c.5196A>C MANE Select ENSP00000495607.1:p.Pro1732=
NM_001145026.1:c.5196A>C NP_001138498.1:p.Pro1732=
ENST00000614701.4:c.5196A>C ENSP00000482885.1:p.Pro1732=
ENST00000616559.4:c.5322A>C ENSP00000483259.1:p.Pro1774=
XM_011538290.1:c.5196A>C XP_011536592.1:p.Pro1732=
XM_017019273.1:c.5862A>C XP_016874762.1:p.Pro1954=
XM_017019274.1:c.5862A>C XP_016874763.1:p.Pro1954=
XM_017019275.1:c.5862A>C XP_016874764.1:p.Pro1954=
XR_001748688.1:n.5999A>C
XR_001748689.1:n.5999A>C
XR_001749222.1:n.121-35823T>G