Canonical Allele Identifier: CA2665985103

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293138-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293139del , CM000665.2:g.52293139del	GRCh38
NC_000003.11:g.52327155del , CM000665.1:g.52327155del	GRCh37
NC_000003.10:g.52302195del	NCBI36
NG_023246.1:g.10320del

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.*13del MANE Select	ENSP00000389175.2:n.*13del
ENST00000436784.6:c.*13del	ENSP00000389175.2:n.*13del
ENST00000461183.5:c.*5del	ENSP00000417264.1:n.*5del
ENST00000471180.5:c.*5del	ENSP00000417526.1:n.*5del
ENST00000473032.5:c.*5del	ENSP00000418951.1:n.*5del
ENST00000486393.5:c.*948del	ENSP00000419868.1:n.*948del
ENST00000489173.1:n.1879del
NM_145262.3:c.*13del	NP_660305.2:n.*13del
NR_026699.1:n.1683del
NR_026700.1:n.789del
NR_026701.1:n.1681del
NR_026702.1:n.719del
XM_005264878.2:c.*704del	XP_005264935.1:n.*704del
XR_245095.2:n.2836del
XM_017005730.1:c.*13del	XP_016861219.1:n.*13del
XM_024453351.1:c.*13del	XP_024309119.1:n.*13del
XM_024453352.1:c.*704del	XP_024309120.1:n.*704del
XR_001740022.2:n.3487del
XR_001740023.2:n.3011del
XR_245095.4:n.2837del
NM_145262.4:c.*13del MANE Select	NP_660305.2:n.*13del
NR_026699.2:n.1675del
NR_026700.2:n.781del
NR_026701.2:n.1673del
NR_026702.2:n.711del
NM_001144951.2:c.*704del	NP_001138423.1:n.*704del