Canonical Allele Identifier: CA480815446

Gene: PTPRQ

Linked Data

• MyVariant Identifiers: chr12:g.80878213T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484434T>G , CM000674.2:g.80484434T>G	GRCh38
NC_000012.11:g.80878213T>G , CM000674.1:g.80878213T>G	GRCh37
NC_000012.10:g.79402344T>G	NCBI36
NG_034052.1:g.45089T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1188T>G MANE Select	ENSP00000495607.1:p.Val396=
ENST00000614701.4:c.1188T>G	ENSP00000482885.1:p.Val396=
ENST00000616559.4:c.1314T>G	ENSP00000483259.1:p.Val438=
NM_001145026.1:c.1188T>G	NP_001138498.1:p.Val396=
XM_011538290.1:c.1188T>G	XP_011536592.1:p.Val396=
XM_017019273.1:c.1854T>G	XP_016874762.1:p.Val618=
XM_017019274.1:c.1854T>G	XP_016874763.1:p.Val618=
XM_017019275.1:c.1854T>G	XP_016874764.1:p.Val618=
XR_001748688.1:n.1991T>G
XR_001748689.1:n.1991T>G
NM_001145026.2:c.1188T>G MANE Select	NP_001138498.1:p.Val396=