Canonical Allele Identifier: CA1364789347
Gene: GLYCTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52293282C= , CM000665.2:g.52293282C= GRCh38
NC_000003.11:g.52327298C= , CM000665.1:g.52327298C= GRCh37
NC_000003.10:g.52302338C= NCBI36
NG_023246.1:g.10463C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.*156C= MANE Select ENSP00000389175.2:n.*156C=
ENST00000436784.6:c.*156C= ENSP00000389175.2:n.*156C=
ENST00000471180.5:c.*59-25C= ENSP00000417526.1:n.*59-25C=
ENST00000473032.5:c.*59-25C= ENSP00000418951.1:n.*59-25C=
ENST00000486393.5:c.*1091C= ENSP00000419868.1:n.*1091C=
ENST00000489173.1:n.1915-25C=
NM_145262.3:c.*156C= NP_660305.2:n.*156C=
NR_026699.1:n.1826C=
NR_026700.1:n.843-25C=
NR_026701.1:n.1735-25C=
NR_026702.1:n.773-25C=
XM_005264878.2:c.*847C= XP_005264935.1:n.*847C=
XR_245095.2:n.2890-25C=
XM_017005730.1:c.*156C= XP_016861219.1:n.*156C=
XM_024453351.1:c.*156C= XP_024309119.1:n.*156C=
XM_024453352.1:c.*847C= XP_024309120.1:n.*847C=
XR_001740022.2:n.3541-25C=
XR_001740023.2:n.3065-25C=
XR_245095.4:n.2891-25C=
NM_145262.4:c.*156C= MANE Select NP_660305.2:n.*156C=
NR_026699.2:n.1818C=
NR_026700.2:n.835-25C=
NR_026701.2:n.1727-25C=
NR_026702.2:n.765-25C=
NM_001144951.2:c.*847C= NP_001138423.1:n.*847C=