Canonical Allele Identifier: CA2665985142

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293224-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293224G>T , CM000665.2:g.52293224G>T	GRCh38
NC_000003.11:g.52327240G>T , CM000665.1:g.52327240G>T	GRCh37
NC_000003.10:g.52302280G>T	NCBI36
NG_023246.1:g.10405G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*98G>T MANE Select	ENSP00000389175.2:n.*98G>T
ENST00000436784.6:c.*98G>T	ENSP00000389175.2:n.*98G>T
ENST00000471180.5:c.*58+32G>T	ENSP00000417526.1:n.*58+32G>T
ENST00000473032.5:c.*58+32G>T	ENSP00000418951.1:n.*58+32G>T
ENST00000486393.5:c.*1033G>T	ENSP00000419868.1:n.*1033G>T
ENST00000489173.1:n.1914+50G>T
NM_145262.3:c.*98G>T	NP_660305.2:n.*98G>T
NR_026699.1:n.1768G>T
NR_026700.1:n.842+32G>T
NR_026701.1:n.1734+32G>T
NR_026702.1:n.772+32G>T
XM_005264878.2:c.*789G>T	XP_005264935.1:n.*789G>T
XR_245095.2:n.2889+32G>T
XM_017005730.1:c.*98G>T	XP_016861219.1:n.*98G>T
XM_024453351.1:c.*98G>T	XP_024309119.1:n.*98G>T
XM_024453352.1:c.*789G>T	XP_024309120.1:n.*789G>T
XR_001740022.2:n.3540+32G>T
XR_001740023.2:n.3064+32G>T
XR_245095.4:n.2890+32G>T
NM_145262.4:c.*98G>T MANE Select	NP_660305.2:n.*98G>T
NR_026699.2:n.1760G>T
NR_026700.2:n.834+32G>T
NR_026701.2:n.1726+32G>T
NR_026702.2:n.764+32G>T
NM_001144951.2:c.*789G>T	NP_001138423.1:n.*789G>T