Canonical Allele Identifier: CA2049270673
Gene: PTPRQ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80484413_80484416delinsTTTC , CM000674.2:g.80484413_80484416delinsTTTC GRCh38
NC_000012.11:g.80878192_80878195delinsTTTC , CM000674.1:g.80878192_80878195delinsTTTC GRCh37
NC_000012.10:g.79402323_79402326delinsTTTC NCBI36
NG_034052.1:g.45068_45071delinsTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000644991.3:c.1187-20_1187-17delinsTTTC MANE Select ENSP00000495607.1:n.1187-20_1187-17delinsTTTC
ENST00000614701.4:c.1187-20_1187-17delinsTTTC ENSP00000482885.1:n.1187-20_1187-17delinsTTTC
ENST00000616559.4:c.1313-20_1313-17delinsTTTC ENSP00000483259.1:n.1313-20_1313-17delinsTTTC
NM_001145026.1:c.1187-20_1187-17delinsTTTC NP_001138498.1:n.1187-20_1187-17delinsTTTC
XM_011538290.1:c.1187-20_1187-17delinsTTTC XP_011536592.1:n.1187-20_1187-17delinsTTTC
XM_017019273.1:c.1853-20_1853-17delinsTTTC XP_016874762.1:n.1853-20_1853-17delinsTTTC
XM_017019274.1:c.1853-20_1853-17delinsTTTC XP_016874763.1:n.1853-20_1853-17delinsTTTC
XM_017019275.1:c.1853-20_1853-17delinsTTTC XP_016874764.1:n.1853-20_1853-17delinsTTTC
XR_001748688.1:n.1990-20_1990-17delinsTTTC
XR_001748689.1:n.1990-20_1990-17delinsTTTC
NM_001145026.2:c.1187-20_1187-17delinsTTTC MANE Select NP_001138498.1:n.1187-20_1187-17delinsTTTC