Canonical Allele Identifier: CA353076003

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326943C>A (hg19) ; chr3:g.52292927C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292927C>A , CM000665.2:g.52292927C>A	GRCh38
NC_000003.11:g.52326943C>A , CM000665.1:g.52326943C>A	GRCh37
NC_000003.10:g.52301983C>A	NCBI36
NG_023246.1:g.10108C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1373C>A MANE Select	ENSP00000389175.2:p.Thr458Lys
ENST00000305690.12:c.*492C>A	ENSP00000301965.9:n.*492C>A
ENST00000436784.6:c.1373C>A	ENSP00000389175.2:p.Thr458Lys
ENST00000461183.5:c.764-119C>A	ENSP00000417264.1:n.764-119C>A
ENST00000471180.5:c.635-119C>A	ENSP00000417526.1:n.635-119C>A
ENST00000473032.5:c.530-119C>A	ENSP00000418951.1:n.530-119C>A
ENST00000477382.1:c.*492C>A	ENSP00000419008.1:n.*492C>A
ENST00000486393.5:c.*736C>A	ENSP00000419868.1:n.*736C>A
ENST00000489173.1:n.1667C>A
NM_001144951.1:c.*492C>A	NP_001138423.1:n.*492C>A
NM_145262.3:c.1373C>A	NP_660305.2:p.Thr458Lys
NR_026699.1:n.1471C>A
NR_026700.1:n.696-119C>A
NR_026701.1:n.1469C>A
NR_026702.1:n.626-119C>A
XM_005264878.2:c.*492C>A	XP_005264935.1:n.*492C>A
XR_245095.2:n.2743-119C>A
XM_017005730.1:c.992C>A	XP_016861219.1:p.Thr331Lys
XM_024453351.1:c.1373C>A	XP_024309119.1:p.Thr458Lys
XM_024453352.1:c.*492C>A	XP_024309120.1:n.*492C>A
XR_001740022.2:n.3275C>A
XR_001740023.2:n.2918-119C>A
XR_245095.4:n.2744-119C>A
NM_145262.4:c.1373C>A MANE Select	NP_660305.2:p.Thr458Lys
NR_026699.2:n.1463C>A
NR_026700.2:n.688-119C>A
NR_026701.2:n.1461C>A
NR_026702.2:n.618-119C>A
NM_001144951.2:c.*492C>A	NP_001138423.1:n.*492C>A