Canonical Allele Identifier: CA1364789214
Gene: GLYCTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52293019T= , CM000665.2:g.52293019T= GRCh38
NC_000003.11:g.52327035T= , CM000665.1:g.52327035T= GRCh37
NC_000003.10:g.52302075T= NCBI36
NG_023246.1:g.10200T=

Transcript Alleles

HGVS Amino-acid change
ENST00000436784.7:c.1465T= MANE Select ENSP00000389175.2:p.Ser489=
ENST00000436784.6:c.1465T= ENSP00000389175.2:p.Ser489=
ENST00000461183.5:c.764-27T= ENSP00000417264.1:n.764-27T=
ENST00000471180.5:c.635-27T= ENSP00000417526.1:n.635-27T=
ENST00000473032.5:c.530-27T= ENSP00000418951.1:n.530-27T=
ENST00000486393.5:c.*828T= ENSP00000419868.1:n.*828T=
ENST00000489173.1:n.1759T=
NM_145262.3:c.1465T= NP_660305.2:p.Ser489=
NR_026699.1:n.1563T=
NR_026700.1:n.696-27T=
NR_026701.1:n.1561T=
NR_026702.1:n.626-27T=
XM_005264878.2:c.*584T= XP_005264935.1:n.*584T=
XR_245095.2:n.2743-27T=
XM_017005730.1:c.1084T= XP_016861219.1:p.Ser362=
XM_024453351.1:c.1465T= XP_024309119.1:p.Ser489=
XM_024453352.1:c.*584T= XP_024309120.1:n.*584T=
XR_001740022.2:n.3367T=
XR_001740023.2:n.2918-27T=
XR_245095.4:n.2744-27T=
NM_145262.4:c.1465T= MANE Select NP_660305.2:p.Ser489=
NR_026699.2:n.1555T=
NR_026700.2:n.688-27T=
NR_026701.2:n.1553T=
NR_026702.2:n.618-27T=
NM_001144951.2:c.*584T= NP_001138423.1:n.*584T=