Canonical Allele Identifier: CA2840119978
Gene: GLYCTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52292818dup , CM000665.2:g.52292818dup GRCh38
NC_000003.11:g.52326834dup , CM000665.1:g.52326834dup GRCh37
NC_000003.10:g.52301874dup NCBI36
NG_023246.1:g.9999dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.1264dup MANE Select ENSP00000389175.2:p.Arg422ProfsTer?
ENST00000305690.12:c.*383dup ENSP00000301965.9:n.*383dup
ENST00000436784.6:c.1264dup ENSP00000389175.2:p.Arg422ProfsTer?
ENST00000461183.5:c.764-228dup ENSP00000417264.1:n.764-228dup
ENST00000471180.5:c.635-228dup ENSP00000417526.1:n.635-228dup
ENST00000473032.5:c.530-228dup ENSP00000418951.1:n.530-228dup
ENST00000477382.1:c.*383dup ENSP00000419008.1:n.*383dup
ENST00000486393.5:c.*627dup ENSP00000419868.1:n.*627dup
ENST00000489173.1:n.1558dup
NM_001144951.1:c.*383dup NP_001138423.1:n.*383dup
NM_145262.3:c.1264dup NP_660305.2:p.Arg422ProfsTer?
NR_026699.1:n.1362dup
NR_026700.1:n.696-228dup
NR_026701.1:n.1360dup
NR_026702.1:n.626-228dup
XM_005264878.2:c.*383dup XP_005264935.1:n.*383dup
XR_245095.2:n.2743-228dup
XM_017005730.1:c.883dup XP_016861219.1:p.Arg295ProfsTer?
XM_024453351.1:c.1264dup XP_024309119.1:p.Arg422ProfsTer?
XM_024453352.1:c.*383dup XP_024309120.1:n.*383dup
XR_001740022.2:n.3166dup
XR_001740023.2:n.2918-228dup
XR_245095.4:n.2744-228dup
NM_145262.4:c.1264dup MANE Select NP_660305.2:p.Arg422ProfsTer?
NR_026699.2:n.1354dup
NR_026700.2:n.688-228dup
NR_026701.2:n.1352dup
NR_026702.2:n.618-228dup
NM_001144951.2:c.*383dup NP_001138423.1:n.*383dup