Canonical Allele Identifier: CA1364789201

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293000_52293001delinsCT , CM000665.2:g.52293000_52293001delinsCT	GRCh38
NC_000003.11:g.52327016_52327017delinsCT , CM000665.1:g.52327016_52327017delinsCT	GRCh37
NC_000003.10:g.52302056_52302057delinsCT	NCBI36
NG_023246.1:g.10181_10182delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1446_1447delinsCT MANE Select	ENSP00000389175.2:p.Thr482=
ENST00000305690.12:c.*565_*566delinsCT	ENSP00000301965.9:n.*565_*566delinsCT
ENST00000436784.6:c.1446_1447delinsCT	ENSP00000389175.2:p.Thr482=
ENST00000461183.5:c.764-46_764-45delinsCT	ENSP00000417264.1:n.764-46_764-45delinsCT
ENST00000471180.5:c.635-46_635-45delinsCT	ENSP00000417526.1:n.635-46_635-45delinsCT
ENST00000473032.5:c.530-46_530-45delinsCT	ENSP00000418951.1:n.530-46_530-45delinsCT
ENST00000477382.1:c.*565_*566delinsCT	ENSP00000419008.1:n.*565_*566delinsCT
ENST00000486393.5:c.*809_*810delinsCT	ENSP00000419868.1:n.*809_*810delinsCT
ENST00000489173.1:n.1740_1741delinsCT
NM_001144951.1:c.*565_*566delinsCT	NP_001138423.1:n.*565_*566delinsCT
NM_145262.3:c.1446_1447delinsCT	NP_660305.2:p.Thr482=
NR_026699.1:n.1544_1545delinsCT
NR_026700.1:n.696-46_696-45delinsCT
NR_026701.1:n.1542_1543delinsCT
NR_026702.1:n.626-46_626-45delinsCT
XM_005264878.2:c.*565_*566delinsCT	XP_005264935.1:n.*565_*566delinsCT
XR_245095.2:n.2743-46_2743-45delinsCT
XM_017005730.1:c.1065_1066delinsCT	XP_016861219.1:p.Thr355=
XM_024453351.1:c.1446_1447delinsCT	XP_024309119.1:p.Thr482=
XM_024453352.1:c.*565_*566delinsCT	XP_024309120.1:n.*565_*566delinsCT
XR_001740022.2:n.3348_3349delinsCT
XR_001740023.2:n.2918-46_2918-45delinsCT
XR_245095.4:n.2744-46_2744-45delinsCT
NM_145262.4:c.1446_1447delinsCT MANE Select	NP_660305.2:p.Thr482=
NR_026699.2:n.1536_1537delinsCT
NR_026700.2:n.688-46_688-45delinsCT
NR_026701.2:n.1534_1535delinsCT
NR_026702.2:n.618-46_618-45delinsCT
NM_001144951.2:c.*565_*566delinsCT	NP_001138423.1:n.*565_*566delinsCT