Canonical Allele Identifier: CA74736952

Gene: GLYCTK

Linked Data

• dbSNP Id: rs971660120
• gnomAD v3: 3-52293316-C-A
• gnomAD v4: 3-52293316-C-A
• MyVariant Identifiers: chr3:g.52327332C>A (hg19) ; chr3:g.52293316C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293316C>A , CM000665.2:g.52293316C>A	GRCh38
NC_000003.11:g.52327332C>A , CM000665.1:g.52327332C>A	GRCh37
NC_000003.10:g.52302372C>A	NCBI36
NG_023246.1:g.10497C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*190C>A MANE Select	ENSP00000389175.2:n.*190C>A
ENST00000436784.6:c.*190C>A	ENSP00000389175.2:n.*190C>A
ENST00000471180.5:c.*68C>A	ENSP00000417526.1:n.*68C>A
ENST00000473032.5:c.*68C>A	ENSP00000418951.1:n.*68C>A
ENST00000486393.5:c.*1125C>A	ENSP00000419868.1:n.*1125C>A
ENST00000489173.1:n.1924C>A
NM_145262.3:c.*190C>A	NP_660305.2:n.*190C>A
NR_026699.1:n.1860C>A
NR_026700.1:n.852C>A
NR_026701.1:n.1744C>A
NR_026702.1:n.782C>A
XM_005264878.2:c.*881C>A	XP_005264935.1:n.*881C>A
XR_245095.2:n.2899C>A
XM_017005730.1:c.*190C>A	XP_016861219.1:n.*190C>A
XM_024453351.1:c.*190C>A	XP_024309119.1:n.*190C>A
XM_024453352.1:c.*881C>A	XP_024309120.1:n.*881C>A
XR_001740022.2:n.3550C>A
XR_001740023.2:n.3074C>A
XR_245095.4:n.2900C>A
NM_145262.4:c.*190C>A MANE Select	NP_660305.2:n.*190C>A
NR_026699.2:n.1852C>A
NR_026700.2:n.844C>A
NR_026701.2:n.1736C>A
NR_026702.2:n.774C>A
NM_001144951.2:c.*881C>A	NP_001138423.1:n.*881C>A