Canonical Allele Identifier: CA2840119983
Gene: GLYCTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52292984del , CM000665.2:g.52292984del GRCh38
NC_000003.11:g.52327000del , CM000665.1:g.52327000del GRCh37
NC_000003.10:g.52302040del NCBI36
NG_023246.1:g.10165del

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.1430del MANE Select ENSP00000389175.2:p.Gly477AlafsTer4
ENST00000305690.12:c.*549del ENSP00000301965.9:n.*549del
ENST00000436784.6:c.1430del ENSP00000389175.2:p.Gly477AlafsTer4
ENST00000461183.5:c.764-62del ENSP00000417264.1:n.764-62del
ENST00000471180.5:c.635-62del ENSP00000417526.1:n.635-62del
ENST00000473032.5:c.530-62del ENSP00000418951.1:n.530-62del
ENST00000477382.1:c.*549del ENSP00000419008.1:n.*549del
ENST00000486393.5:c.*793del ENSP00000419868.1:n.*793del
ENST00000489173.1:n.1724del
NM_001144951.1:c.*549del NP_001138423.1:n.*549del
NM_145262.3:c.1430del NP_660305.2:p.Gly477AlafsTer4
NR_026699.1:n.1528del
NR_026700.1:n.696-62del
NR_026701.1:n.1526del
NR_026702.1:n.626-62del
XM_005264878.2:c.*549del XP_005264935.1:n.*549del
XR_245095.2:n.2743-62del
XM_017005730.1:c.1049del XP_016861219.1:p.Gly350AlafsTer4
XM_024453351.1:c.1430del XP_024309119.1:p.Gly477AlafsTer4
XM_024453352.1:c.*549del XP_024309120.1:n.*549del
XR_001740022.2:n.3332del
XR_001740023.2:n.2918-62del
XR_245095.4:n.2744-62del
NM_145262.4:c.1430del MANE Select NP_660305.2:p.Gly477AlafsTer4
NR_026699.2:n.1520del
NR_026700.2:n.688-62del
NR_026701.2:n.1518del
NR_026702.2:n.618-62del
NM_001144951.2:c.*549del NP_001138423.1:n.*549del