Canonical Allele Identifier: CA2049256745

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80460595_80460596delinsCT , CM000674.2:g.80460595_80460596delinsCT	GRCh38
NC_000012.11:g.80849581_80849582delinsAG , CM000674.1:g.80849581_80849582delinsAG	GRCh37
NC_000012.10:g.79373712_79373713delinsAG	NCBI36
NG_034052.1:g.21250_21251delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.661-58_661-57delinsCT MANE Select	ENSP00000495607.1:n.661-58_661-57delinsCT
ENST00000614701.4:c.661-58_661-57delinsCT	ENSP00000482885.1:n.661-58_661-57delinsCT
ENST00000616559.4:c.787-58_787-57delinsCT	ENSP00000483259.1:n.787-58_787-57delinsCT
NM_001145026.1:c.661-58_661-57delinsCT	NP_001138498.1:n.661-58_661-57delinsCT
XM_011538290.1:c.661-58_661-57delinsCT	XP_011536592.1:n.661-58_661-57delinsCT
XM_017019273.1:c.1327-58_1327-57delinsCT	XP_016874762.1:n.1327-58_1327-57delinsCT
XM_017019274.1:c.1327-58_1327-57delinsCT	XP_016874763.1:n.1327-58_1327-57delinsCT
XM_017019275.1:c.1327-58_1327-57delinsCT	XP_016874764.1:n.1327-58_1327-57delinsCT
XR_001748688.1:n.1464-58_1464-57delinsCT
XR_001748689.1:n.1464-58_1464-57delinsCT
NM_001145026.2:c.661-58_661-57delinsCT MANE Select	NP_001138498.1:n.661-58_661-57delinsCT