Canonical Allele Identifier: CA2665986948
Gene: GLYCTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52293078del , CM000665.2:g.52293078del GRCh38
NC_000003.11:g.52327094del , CM000665.1:g.52327094del GRCh37
NC_000003.10:g.52302134del NCBI36
NG_023246.1:g.10259del

Transcript Alleles

HGVS Amino-acid change
ENST00000436784.7:c.1524del MANE Select ENSP00000389175.2:p.Gly509ValfsTer?
ENST00000436784.6:c.1524del ENSP00000389175.2:p.Gly509ValfsTer?
ENST00000461183.5:c.796del ENSP00000417264.1:p.Arg266GlyfsTer16
ENST00000471180.5:c.667del ENSP00000417526.1:p.Arg223GlyfsTer16
ENST00000473032.5:c.562del ENSP00000418951.1:p.Arg188GlyfsTer16
ENST00000486393.5:c.*887del ENSP00000419868.1:n.*887del
ENST00000489173.1:n.1818del
NM_145262.3:c.1524del NP_660305.2:p.Gly509ValfsTer?
NR_026699.1:n.1622del
NR_026700.1:n.728del
NR_026701.1:n.1620del
NR_026702.1:n.658del
XM_005264878.2:c.*643del XP_005264935.1:n.*643del
XR_245095.2:n.2775del
XM_017005730.1:c.1143del XP_016861219.1:p.Gly382ValfsTer?
XM_024453351.1:c.1524del XP_024309119.1:p.Gly509ValfsTer?
XM_024453352.1:c.*643del XP_024309120.1:n.*643del
XR_001740022.2:n.3426del
XR_001740023.2:n.2950del
XR_245095.4:n.2776del
NM_145262.4:c.1524del MANE Select NP_660305.2:p.Gly509ValfsTer?
NR_026699.2:n.1614del
NR_026700.2:n.720del
NR_026701.2:n.1612del
NR_026702.2:n.650del
NM_001144951.2:c.*643del NP_001138423.1:n.*643del