Canonical Allele Identifier: CA2049270662

Gene: PTPRQ

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80484403_80484407delinsTTTTC , CM000674.2:g.80484403_80484407delinsTTTTC	GRCh38
NC_000012.11:g.80878182_80878186delinsTTTTC , CM000674.1:g.80878182_80878186delinsTTTTC	GRCh37
NC_000012.10:g.79402313_79402317delinsTTTTC	NCBI36
NG_034052.1:g.45058_45062delinsTTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644991.3:c.1187-30_1187-26delinsTTTTC MANE Select	ENSP00000495607.1:n.1187-30_1187-26delinsTTTTC
ENST00000614701.4:c.1187-30_1187-26delinsTTTTC	ENSP00000482885.1:n.1187-30_1187-26delinsTTTTC
ENST00000616559.4:c.1313-30_1313-26delinsTTTTC	ENSP00000483259.1:n.1313-30_1313-26delinsTTTTC
NM_001145026.1:c.1187-30_1187-26delinsTTTTC	NP_001138498.1:n.1187-30_1187-26delinsTTTTC
XM_011538290.1:c.1187-30_1187-26delinsTTTTC	XP_011536592.1:n.1187-30_1187-26delinsTTTTC
XM_017019273.1:c.1853-30_1853-26delinsTTTTC	XP_016874762.1:n.1853-30_1853-26delinsTTTTC
XM_017019274.1:c.1853-30_1853-26delinsTTTTC	XP_016874763.1:n.1853-30_1853-26delinsTTTTC
XM_017019275.1:c.1853-30_1853-26delinsTTTTC	XP_016874764.1:n.1853-30_1853-26delinsTTTTC
XR_001748688.1:n.1990-30_1990-26delinsTTTTC
XR_001748689.1:n.1990-30_1990-26delinsTTTTC
NM_001145026.2:c.1187-30_1187-26delinsTTTTC MANE Select	NP_001138498.1:n.1187-30_1187-26delinsTTTTC