Canonical Allele Identifier: CA2620022608

Gene: PTPRQ

Linked Data

• gnomAD v4: 12-80460597-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460597T>A , CM000674.2:g.80460597T>A	GRCh38
NC_000012.11:g.80849580A>T , CM000674.1:g.80849580A>T	GRCh37
NC_000012.10:g.79373711A>T	NCBI36
NG_034052.1:g.21252T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.661-56T>A MANE Select	ENSP00000495607.1:n.661-56T>A
ENST00000614701.4:c.661-56T>A	ENSP00000482885.1:n.661-56T>A
ENST00000616559.4:c.787-56T>A	ENSP00000483259.1:n.787-56T>A
NM_001145026.1:c.661-56T>A	NP_001138498.1:n.661-56T>A
XM_011538290.1:c.661-56T>A	XP_011536592.1:n.661-56T>A
XM_017019273.1:c.1327-56T>A	XP_016874762.1:n.1327-56T>A
XM_017019274.1:c.1327-56T>A	XP_016874763.1:n.1327-56T>A
XM_017019275.1:c.1327-56T>A	XP_016874764.1:n.1327-56T>A
XR_001748688.1:n.1464-56T>A
XR_001748689.1:n.1464-56T>A
NM_001145026.2:c.661-56T>A MANE Select	NP_001138498.1:n.661-56T>A