Canonical Allele Identifier: CA10605280
Gene: PTPRQ HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80620153G>T , CM000674.2:g.80620153G>T GRCh38
NC_000012.11:g.81013932G>T , CM000674.1:g.81013932G>T GRCh37
NC_000012.10:g.79538063G>T NCBI36
NG_034052.1:g.180808G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000644991.3:c.5390-1G>T MANE Select ENSP00000495607.1:n.5390-1G>T
ENST00000614701.4:c.5390-1G>T ENSP00000482885.1:n.5390-1G>T
ENST00000616559.4:c.5516-1G>T ENSP00000483259.1:n.5516-1G>T
NM_001145026.1:c.5390-1G>T NP_001138498.1:n.5390-1G>T
XM_011538290.1:c.5390-1G>T XP_011536592.1:n.5390-1G>T
XM_017019273.1:c.6056-1G>T XP_016874762.1:n.6056-1G>T
XM_017019274.1:c.6056-1G>T XP_016874763.1:n.6056-1G>T
XM_017019275.1:c.6056-1G>T XP_016874764.1:n.6056-1G>T
XR_001748688.1:n.6193-1G>T
XR_001748689.1:n.6193-1G>T
XR_001749222.1:n.121-39744C>A
NM_001145026.2:c.5390-1G>T MANE Select NP_001138498.1:n.5390-1G>T
Search 100 bp 5'
Search 100 bp 3'