Canonical Allele Identifier: CA385884098

Gene: PTPRQ

Linked Data

• MyVariant Identifiers: chr12:g.80878341C>A (hg19) ; chr12:g.80484562C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484562C>A , CM000674.2:g.80484562C>A	GRCh38
NC_000012.11:g.80878341C>A , CM000674.1:g.80878341C>A	GRCh37
NC_000012.10:g.79402472C>A	NCBI36
NG_034052.1:g.45217C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1316C>A MANE Select	ENSP00000495607.1:p.Thr439Lys
ENST00000614701.4:c.1316C>A	ENSP00000482885.1:p.Thr439Lys
ENST00000616559.4:c.1442C>A	ENSP00000483259.1:p.Thr481Lys
NM_001145026.1:c.1316C>A	NP_001138498.1:p.Thr439Lys
XM_011538290.1:c.1316C>A	XP_011536592.1:p.Thr439Lys
XM_017019273.1:c.1982C>A	XP_016874762.1:p.Thr661Lys
XM_017019274.1:c.1982C>A	XP_016874763.1:p.Thr661Lys
XM_017019275.1:c.1982C>A	XP_016874764.1:p.Thr661Lys
XR_001748688.1:n.2119C>A
XR_001748689.1:n.2119C>A
NM_001145026.2:c.1316C>A MANE Select	NP_001138498.1:p.Thr439Lys