Canonical Allele Identifier: CA2665986836
Gene: GLYCTK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52293047_52293053del , CM000665.2:g.52293047_52293053del GRCh38
NC_000003.11:g.52327063_52327069del , CM000665.1:g.52327063_52327069del GRCh37
NC_000003.10:g.52302103_52302109del NCBI36
NG_023246.1:g.10228_10234del

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.1493_1499del MANE Select ENSP00000389175.2:p.Gly498AspfsTer8
ENST00000436784.6:c.1493_1499del ENSP00000389175.2:p.Gly498AspfsTer8
ENST00000461183.5:c.765_771del ENSP00000417264.1:p.Trp256HisfsTer24
ENST00000471180.5:c.636_642del ENSP00000417526.1:p.Trp213HisfsTer24
ENST00000473032.5:c.531_537del ENSP00000418951.1:p.Trp178HisfsTer24
ENST00000486393.5:c.*856_*862del ENSP00000419868.1:n.*856_*862del
ENST00000489173.1:n.1787_1793del
NM_145262.3:c.1493_1499del NP_660305.2:p.Gly498AspfsTer8
NR_026699.1:n.1591_1597del
NR_026700.1:n.697_703del
NR_026701.1:n.1589_1595del
NR_026702.1:n.627_633del
XM_005264878.2:c.*612_*618del XP_005264935.1:n.*612_*618del
XR_245095.2:n.2744_2750del
XM_017005730.1:c.1112_1118del XP_016861219.1:p.Gly371AspfsTer8
XM_024453351.1:c.1493_1499del XP_024309119.1:p.Gly498AspfsTer8
XM_024453352.1:c.*612_*618del XP_024309120.1:n.*612_*618del
XR_001740022.2:n.3395_3401del
XR_001740023.2:n.2919_2925del
XR_245095.4:n.2745_2751del
NM_145262.4:c.1493_1499del MANE Select NP_660305.2:p.Gly498AspfsTer8
NR_026699.2:n.1583_1589del
NR_026700.2:n.689_695del
NR_026701.2:n.1581_1587del
NR_026702.2:n.619_625del
NM_001144951.2:c.*612_*618del NP_001138423.1:n.*612_*618del