Canonical Allele Identifier: CA1364789220
Gene: GLYCTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52293026_52293029delinsCCTT , CM000665.2:g.52293026_52293029delinsCCTT GRCh38
NC_000003.11:g.52327042_52327045delinsCCTT , CM000665.1:g.52327042_52327045delinsCCTT GRCh37
NC_000003.10:g.52302082_52302085delinsCCTT NCBI36
NG_023246.1:g.10207_10210delinsCCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.1472_1475delinsCCTT MANE Select ENSP00000389175.2:p.Thr491=
ENST00000436784.6:c.1472_1475delinsCCTT ENSP00000389175.2:p.Thr491=
ENST00000461183.5:c.764-20_764-17delinsCCTT ENSP00000417264.1:n.764-20_764-17delinsCCTT
ENST00000471180.5:c.635-20_635-17delinsCCTT ENSP00000417526.1:n.635-20_635-17delinsCCTT
ENST00000473032.5:c.530-20_530-17delinsCCTT ENSP00000418951.1:n.530-20_530-17delinsCCTT
ENST00000486393.5:c.*835_*838delinsCCTT ENSP00000419868.1:n.*835_*838delinsCCTT
ENST00000489173.1:n.1766_1769delinsCCTT
NM_145262.3:c.1472_1475delinsCCTT NP_660305.2:p.Thr491=
NR_026699.1:n.1570_1573delinsCCTT
NR_026700.1:n.696-20_696-17delinsCCTT
NR_026701.1:n.1568_1571delinsCCTT
NR_026702.1:n.626-20_626-17delinsCCTT
XM_005264878.2:c.*591_*594delinsCCTT XP_005264935.1:n.*591_*594delinsCCTT
XR_245095.2:n.2743-20_2743-17delinsCCTT
XM_017005730.1:c.1091_1094delinsCCTT XP_016861219.1:p.Thr364=
XM_024453351.1:c.1472_1475delinsCCTT XP_024309119.1:p.Thr491=
XM_024453352.1:c.*591_*594delinsCCTT XP_024309120.1:n.*591_*594delinsCCTT
XR_001740022.2:n.3374_3377delinsCCTT
XR_001740023.2:n.2918-20_2918-17delinsCCTT
XR_245095.4:n.2744-20_2744-17delinsCCTT
NM_145262.4:c.1472_1475delinsCCTT MANE Select NP_660305.2:p.Thr491=
NR_026699.2:n.1562_1565delinsCCTT
NR_026700.2:n.688-20_688-17delinsCCTT
NR_026701.2:n.1560_1563delinsCCTT
NR_026702.2:n.618-20_618-17delinsCCTT
NM_001144951.2:c.*591_*594delinsCCTT NP_001138423.1:n.*591_*594delinsCCTT