Canonical Allele Identifier: CA2665985131

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293207-CCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293212_52293213del , CM000665.2:g.52293212_52293213del	GRCh38
NC_000003.11:g.52327228_52327229del , CM000665.1:g.52327228_52327229del	GRCh37
NC_000003.10:g.52302268_52302269del	NCBI36
NG_023246.1:g.10393_10394del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*86_*87del MANE Select	ENSP00000389175.2:n.*86_*87del
ENST00000436784.6:c.*86_*87del	ENSP00000389175.2:n.*86_*87del
ENST00000471180.5:c.*58+20_*58+21del	ENSP00000417526.1:n.*58+20_*58+21del
ENST00000473032.5:c.*58+20_*58+21del	ENSP00000418951.1:n.*58+20_*58+21del
ENST00000486393.5:c.*1021_*1022del	ENSP00000419868.1:n.*1021_*1022del
ENST00000489173.1:n.1914+38_1914+39del
NM_145262.3:c.*86_*87del	NP_660305.2:n.*86_*87del
NR_026699.1:n.1756_1757del
NR_026700.1:n.842+20_842+21del
NR_026701.1:n.1734+20_1734+21del
NR_026702.1:n.772+20_772+21del
XM_005264878.2:c.*777_*778del	XP_005264935.1:n.*777_*778del
XR_245095.2:n.2889+20_2889+21del
XM_017005730.1:c.*86_*87del	XP_016861219.1:n.*86_*87del
XM_024453351.1:c.*86_*87del	XP_024309119.1:n.*86_*87del
XM_024453352.1:c.*777_*778del	XP_024309120.1:n.*777_*778del
XR_001740022.2:n.3540+20_3540+21del
XR_001740023.2:n.3064+20_3064+21del
XR_245095.4:n.2890+20_2890+21del
NM_145262.4:c.*86_*87del MANE Select	NP_660305.2:n.*86_*87del
NR_026699.2:n.1748_1749del
NR_026700.2:n.834+20_834+21del
NR_026701.2:n.1726+20_1726+21del
NR_026702.2:n.764+20_764+21del
NM_001144951.2:c.*777_*778del	NP_001138423.1:n.*777_*778del