Canonical Allele Identifier: CA2577780411
Gene: GLYCTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52292862del , CM000665.2:g.52292862del GRCh38
NC_000003.11:g.52326878del , CM000665.1:g.52326878del GRCh37
NC_000003.10:g.52301918del NCBI36
NG_023246.1:g.10043del

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.1308del MANE Select ENSP00000389175.2:p.Arg436SerfsTer7
ENST00000305690.12:c.*427del ENSP00000301965.9:n.*427del
ENST00000436784.6:c.1308del ENSP00000389175.2:p.Arg436SerfsTer7
ENST00000461183.5:c.764-184del ENSP00000417264.1:n.764-184del
ENST00000471180.5:c.635-184del ENSP00000417526.1:n.635-184del
ENST00000473032.5:c.530-184del ENSP00000418951.1:n.530-184del
ENST00000477382.1:c.*427del ENSP00000419008.1:n.*427del
ENST00000486393.5:c.*671del ENSP00000419868.1:n.*671del
ENST00000489173.1:n.1602del
NM_001144951.1:c.*427del NP_001138423.1:n.*427del
NM_145262.3:c.1308del NP_660305.2:p.Arg436SerfsTer7
NR_026699.1:n.1406del
NR_026700.1:n.696-184del
NR_026701.1:n.1404del
NR_026702.1:n.626-184del
XM_005264878.2:c.*427del XP_005264935.1:n.*427del
XR_245095.2:n.2743-184del
XM_017005730.1:c.927del XP_016861219.1:p.Arg309SerfsTer7
XM_024453351.1:c.1308del XP_024309119.1:p.Arg436SerfsTer7
XM_024453352.1:c.*427del XP_024309120.1:n.*427del
XR_001740022.2:n.3210del
XR_001740023.2:n.2918-184del
XR_245095.4:n.2744-184del
NM_145262.4:c.1308del MANE Select NP_660305.2:p.Arg436SerfsTer7
NR_026699.2:n.1398del
NR_026700.2:n.688-184del
NR_026701.2:n.1396del
NR_026702.2:n.618-184del
NM_001144951.2:c.*427del NP_001138423.1:n.*427del