Canonical Allele Identifier: CA385875568

Gene: PTPRQ

Linked Data

• MyVariant Identifiers: chr12:g.80460657A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460657A>C , CM000674.2:g.80460657A>C	GRCh38
NC_000012.11:g.80849520T>G , CM000674.1:g.80849520T>G	GRCh37
NC_000012.10:g.79373651T>G	NCBI36
NG_034052.1:g.21312A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.665A>C MANE Select	ENSP00000495607.1:p.Asn222Thr
ENST00000614701.4:c.665A>C	ENSP00000482885.1:p.Asn222Thr
ENST00000616559.4:c.791A>C	ENSP00000483259.1:p.Asn264Thr
NM_001145026.1:c.665A>C	NP_001138498.1:p.Asn222Thr
XM_011538290.1:c.665A>C	XP_011536592.1:p.Asn222Thr
XM_017019273.1:c.1331A>C	XP_016874762.1:p.Asn444Thr
XM_017019274.1:c.1331A>C	XP_016874763.1:p.Asn444Thr
XM_017019275.1:c.1331A>C	XP_016874764.1:p.Asn444Thr
XR_001748688.1:n.1468A>C
XR_001748689.1:n.1468A>C
NM_001145026.2:c.665A>C MANE Select	NP_001138498.1:p.Asn222Thr