Canonical Allele Identifier: CA2665985164
Gene: GLYCTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52293257_52293260del , CM000665.2:g.52293257_52293260del GRCh38
NC_000003.11:g.52327273_52327276del , CM000665.1:g.52327273_52327276del GRCh37
NC_000003.10:g.52302313_52302316del NCBI36
NG_023246.1:g.10438_10441del

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.*131_*134del MANE Select ENSP00000389175.2:n.*131_*134del
ENST00000436784.6:c.*131_*134del ENSP00000389175.2:n.*131_*134del
ENST00000471180.5:c.*59-50_*59-47del ENSP00000417526.1:n.*59-50_*59-47del
ENST00000473032.5:c.*59-50_*59-47del ENSP00000418951.1:n.*59-50_*59-47del
ENST00000486393.5:c.*1066_*1069del ENSP00000419868.1:n.*1066_*1069del
ENST00000489173.1:n.1915-50_1915-47del
NM_145262.3:c.*131_*134del NP_660305.2:n.*131_*134del
NR_026699.1:n.1801_1804del
NR_026700.1:n.843-50_843-47del
NR_026701.1:n.1735-50_1735-47del
NR_026702.1:n.773-50_773-47del
XM_005264878.2:c.*822_*825del XP_005264935.1:n.*822_*825del
XR_245095.2:n.2890-50_2890-47del
XM_017005730.1:c.*131_*134del XP_016861219.1:n.*131_*134del
XM_024453351.1:c.*131_*134del XP_024309119.1:n.*131_*134del
XM_024453352.1:c.*822_*825del XP_024309120.1:n.*822_*825del
XR_001740022.2:n.3541-50_3541-47del
XR_001740023.2:n.3065-50_3065-47del
XR_245095.4:n.2891-50_2891-47del
NM_145262.4:c.*131_*134del MANE Select NP_660305.2:n.*131_*134del
NR_026699.2:n.1793_1796del
NR_026700.2:n.835-50_835-47del
NR_026701.2:n.1727-50_1727-47del
NR_026702.2:n.765-50_765-47del
NM_001144951.2:c.*822_*825del NP_001138423.1:n.*822_*825del