Canonical Allele Identifier: CA1364789203

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293002_52293003delinsTC , CM000665.2:g.52293002_52293003delinsTC	GRCh38
NC_000003.11:g.52327018_52327019delinsTC , CM000665.1:g.52327018_52327019delinsTC	GRCh37
NC_000003.10:g.52302058_52302059delinsTC	NCBI36
NG_023246.1:g.10183_10184delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1448_1449delinsTC MANE Select	ENSP00000389175.2:p.Phe483=
ENST00000305690.12:c.*567_*568delinsTC	ENSP00000301965.9:n.*567_*568delinsTC
ENST00000436784.6:c.1448_1449delinsTC	ENSP00000389175.2:p.Phe483=
ENST00000461183.5:c.764-44_764-43delinsTC	ENSP00000417264.1:n.764-44_764-43delinsTC
ENST00000471180.5:c.635-44_635-43delinsTC	ENSP00000417526.1:n.635-44_635-43delinsTC
ENST00000473032.5:c.530-44_530-43delinsTC	ENSP00000418951.1:n.530-44_530-43delinsTC
ENST00000477382.1:c.*567_*568delinsTC	ENSP00000419008.1:n.*567_*568delinsTC
ENST00000486393.5:c.*811_*812delinsTC	ENSP00000419868.1:n.*811_*812delinsTC
ENST00000489173.1:n.1742_1743delinsTC
NM_001144951.1:c.*567_*568delinsTC	NP_001138423.1:n.*567_*568delinsTC
NM_145262.3:c.1448_1449delinsTC	NP_660305.2:p.Phe483=
NR_026699.1:n.1546_1547delinsTC
NR_026700.1:n.696-44_696-43delinsTC
NR_026701.1:n.1544_1545delinsTC
NR_026702.1:n.626-44_626-43delinsTC
XM_005264878.2:c.*567_*568delinsTC	XP_005264935.1:n.*567_*568delinsTC
XR_245095.2:n.2743-44_2743-43delinsTC
XM_017005730.1:c.1067_1068delinsTC	XP_016861219.1:p.Phe356=
XM_024453351.1:c.1448_1449delinsTC	XP_024309119.1:p.Phe483=
XM_024453352.1:c.*567_*568delinsTC	XP_024309120.1:n.*567_*568delinsTC
XR_001740022.2:n.3350_3351delinsTC
XR_001740023.2:n.2918-44_2918-43delinsTC
XR_245095.4:n.2744-44_2744-43delinsTC
NM_145262.4:c.1448_1449delinsTC MANE Select	NP_660305.2:p.Phe483=
NR_026699.2:n.1538_1539delinsTC
NR_026700.2:n.688-44_688-43delinsTC
NR_026701.2:n.1536_1537delinsTC
NR_026702.2:n.618-44_618-43delinsTC
NM_001144951.2:c.*567_*568delinsTC	NP_001138423.1:n.*567_*568delinsTC