Canonical Allele Identifier: CA385883466

Gene: PTPRQ

Linked Data

• gnomAD v4: 12-80484438-G-T
• MyVariant Identifiers: chr12:g.80878217G>T (hg19) ; chr12:g.80484438G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484438G>T , CM000674.2:g.80484438G>T	GRCh38
NC_000012.11:g.80878217G>T , CM000674.1:g.80878217G>T	GRCh37
NC_000012.10:g.79402348G>T	NCBI36
NG_034052.1:g.45093G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000644991.3:c.1192G>T MANE Select	ENSP00000495607.1:p.Gly398Trp
ENST00000614701.4:c.1192G>T	ENSP00000482885.1:p.Gly398Trp
ENST00000616559.4:c.1318G>T	ENSP00000483259.1:p.Gly440Trp
NM_001145026.1:c.1192G>T	NP_001138498.1:p.Gly398Trp
XM_011538290.1:c.1192G>T	XP_011536592.1:p.Gly398Trp
XM_017019273.1:c.1858G>T	XP_016874762.1:p.Gly620Trp
XM_017019274.1:c.1858G>T	XP_016874763.1:p.Gly620Trp
XM_017019275.1:c.1858G>T	XP_016874764.1:p.Gly620Trp
XR_001748688.1:n.1995G>T
XR_001748689.1:n.1995G>T
NM_001145026.2:c.1192G>T MANE Select	NP_001138498.1:p.Gly398Trp