Canonical Allele Identifier: CA480815448

Gene: PTPRQ

Linked Data

• MyVariant Identifiers: chr12:g.80878216A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484437A>C , CM000674.2:g.80484437A>C	GRCh38
NC_000012.11:g.80878216A>C , CM000674.1:g.80878216A>C	GRCh37
NC_000012.10:g.79402347A>C	NCBI36
NG_034052.1:g.45092A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000644991.3:c.1191A>C MANE Select	ENSP00000495607.1:p.Pro397=
ENST00000614701.4:c.1191A>C	ENSP00000482885.1:p.Pro397=
ENST00000616559.4:c.1317A>C	ENSP00000483259.1:p.Pro439=
NM_001145026.1:c.1191A>C	NP_001138498.1:p.Pro397=
XM_011538290.1:c.1191A>C	XP_011536592.1:p.Pro397=
XM_017019273.1:c.1857A>C	XP_016874762.1:p.Pro619=
XM_017019274.1:c.1857A>C	XP_016874763.1:p.Pro619=
XM_017019275.1:c.1857A>C	XP_016874764.1:p.Pro619=
XR_001748688.1:n.1994A>C
XR_001748689.1:n.1994A>C
NM_001145026.2:c.1191A>C MANE Select	NP_001138498.1:p.Pro397=