Canonical Allele Identifier: CA433752122

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327177C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293161C>A , CM000665.2:g.52293161C>A	GRCh38
NC_000003.11:g.52327177C>A , CM000665.1:g.52327177C>A	GRCh37
NC_000003.10:g.52302217C>A	NCBI36
NG_023246.1:g.10342C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*35C>A MANE Select	ENSP00000389175.2:n.*35C>A
ENST00000436784.6:c.*35C>A	ENSP00000389175.2:n.*35C>A
ENST00000461183.5:c.*27C>A	ENSP00000417264.1:n.*27C>A
ENST00000471180.5:c.*27C>A	ENSP00000417526.1:n.*27C>A
ENST00000473032.5:c.*27C>A	ENSP00000418951.1:n.*27C>A
ENST00000486393.5:c.*970C>A	ENSP00000419868.1:n.*970C>A
ENST00000489173.1:n.1901C>A
NM_145262.3:c.*35C>A	NP_660305.2:n.*35C>A
NR_026699.1:n.1705C>A
NR_026700.1:n.811C>A
NR_026701.1:n.1703C>A
NR_026702.1:n.741C>A
XM_005264878.2:c.*726C>A	XP_005264935.1:n.*726C>A
XR_245095.2:n.2858C>A
XM_017005730.1:c.*35C>A	XP_016861219.1:n.*35C>A
XM_024453351.1:c.*35C>A	XP_024309119.1:n.*35C>A
XM_024453352.1:c.*726C>A	XP_024309120.1:n.*726C>A
XR_001740022.2:n.3509C>A
XR_001740023.2:n.3033C>A
XR_245095.4:n.2859C>A
NM_145262.4:c.*35C>A MANE Select	NP_660305.2:n.*35C>A
NR_026699.2:n.1697C>A
NR_026700.2:n.803C>A
NR_026701.2:n.1695C>A
NR_026702.2:n.733C>A
NM_001144951.2:c.*726C>A	NP_001138423.1:n.*726C>A