Canonical Allele Identifier: CA74736924

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1039651830
• gnomAD v3: 3-52293203-A-G
• gnomAD v4: 3-52293203-A-G
• MyVariant Identifiers: chr3:g.52327219A>G (hg19) ; chr3:g.52293203A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293203A>G , CM000665.2:g.52293203A>G	GRCh38
NC_000003.11:g.52327219A>G , CM000665.1:g.52327219A>G	GRCh37
NC_000003.10:g.52302259A>G	NCBI36
NG_023246.1:g.10384A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*77A>G MANE Select	ENSP00000389175.2:n.*77A>G
ENST00000436784.6:c.*77A>G	ENSP00000389175.2:n.*77A>G
ENST00000471180.5:c.*58+11A>G	ENSP00000417526.1:n.*58+11A>G
ENST00000473032.5:c.*58+11A>G	ENSP00000418951.1:n.*58+11A>G
ENST00000486393.5:c.*1012A>G	ENSP00000419868.1:n.*1012A>G
ENST00000489173.1:n.1914+29A>G
NM_145262.3:c.*77A>G	NP_660305.2:n.*77A>G
NR_026699.1:n.1747A>G
NR_026700.1:n.842+11A>G
NR_026701.1:n.1734+11A>G
NR_026702.1:n.772+11A>G
XM_005264878.2:c.*768A>G	XP_005264935.1:n.*768A>G
XR_245095.2:n.2889+11A>G
XM_017005730.1:c.*77A>G	XP_016861219.1:n.*77A>G
XM_024453351.1:c.*77A>G	XP_024309119.1:n.*77A>G
XM_024453352.1:c.*768A>G	XP_024309120.1:n.*768A>G
XR_001740022.2:n.3540+11A>G
XR_001740023.2:n.3064+11A>G
XR_245095.4:n.2890+11A>G
NM_145262.4:c.*77A>G MANE Select	NP_660305.2:n.*77A>G
NR_026699.2:n.1739A>G
NR_026700.2:n.834+11A>G
NR_026701.2:n.1726+11A>G
NR_026702.2:n.764+11A>G
NM_001144951.2:c.*768A>G	NP_001138423.1:n.*768A>G