Canonical Allele Identifier: CA2840119984
Gene: GLYCTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52293062_52293064del , CM000665.2:g.52293062_52293064del GRCh38
NC_000003.11:g.52327078_52327080del , CM000665.1:g.52327078_52327080del GRCh37
NC_000003.10:g.52302118_52302120del NCBI36
NG_023246.1:g.10243_10245del

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.1508_1510del MANE Select ENSP00000389175.2:p.Leu503del
ENST00000436784.6:c.1508_1510del ENSP00000389175.2:p.Leu503del
ENST00000461183.5:c.780_782del ENSP00000417264.1:p.Ala261del
ENST00000471180.5:c.651_653del ENSP00000417526.1:p.Ala218del
ENST00000473032.5:c.546_548del ENSP00000418951.1:p.Ala183del
ENST00000486393.5:c.*871_*873del ENSP00000419868.1:n.*871_*873del
ENST00000489173.1:n.1802_1804del
NM_145262.3:c.1508_1510del NP_660305.2:p.Leu503del
NR_026699.1:n.1606_1608del
NR_026700.1:n.712_714del
NR_026701.1:n.1604_1606del
NR_026702.1:n.642_644del
XM_005264878.2:c.*627_*629del XP_005264935.1:n.*627_*629del
XR_245095.2:n.2759_2761del
XM_017005730.1:c.1127_1129del XP_016861219.1:p.Leu376del
XM_024453351.1:c.1508_1510del XP_024309119.1:p.Leu503del
XM_024453352.1:c.*627_*629del XP_024309120.1:n.*627_*629del
XR_001740022.2:n.3410_3412del
XR_001740023.2:n.2934_2936del
XR_245095.4:n.2760_2762del
NM_145262.4:c.1508_1510del MANE Select NP_660305.2:p.Leu503del
NR_026699.2:n.1598_1600del
NR_026700.2:n.704_706del
NR_026701.2:n.1596_1598del
NR_026702.2:n.634_636del
NM_001144951.2:c.*627_*629del NP_001138423.1:n.*627_*629del