Canonical Allele Identifier: CA353076916

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327134C>A (hg19) ; chr3:g.52293118C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293118C>A , CM000665.2:g.52293118C>A	GRCh38
NC_000003.11:g.52327134C>A , CM000665.1:g.52327134C>A	GRCh37
NC_000003.10:g.52302174C>A	NCBI36
NG_023246.1:g.10299C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1564C>A MANE Select	ENSP00000389175.2:p.Pro522Thr
ENST00000436784.6:c.1564C>A	ENSP00000389175.2:p.Pro522Thr
ENST00000461183.5:c.836C>A	ENSP00000417264.1:p.Ala279Asp
ENST00000471180.5:c.707C>A	ENSP00000417526.1:p.Ala236Asp
ENST00000473032.5:c.602C>A	ENSP00000418951.1:p.Ala201Asp
ENST00000486393.5:c.*927C>A	ENSP00000419868.1:n.*927C>A
ENST00000489173.1:n.1858C>A
NM_145262.3:c.1564C>A	NP_660305.2:p.Pro522Thr
NR_026699.1:n.1662C>A
NR_026700.1:n.768C>A
NR_026701.1:n.1660C>A
NR_026702.1:n.698C>A
XM_005264878.2:c.*683C>A	XP_005264935.1:n.*683C>A
XR_245095.2:n.2815C>A
XM_017005730.1:c.1183C>A	XP_016861219.1:p.Pro395Thr
XM_024453351.1:c.1564C>A	XP_024309119.1:p.Pro522Thr
XM_024453352.1:c.*683C>A	XP_024309120.1:n.*683C>A
XR_001740022.2:n.3466C>A
XR_001740023.2:n.2990C>A
XR_245095.4:n.2816C>A
NM_145262.4:c.1564C>A MANE Select	NP_660305.2:p.Pro522Thr
NR_026699.2:n.1654C>A
NR_026700.2:n.760C>A
NR_026701.2:n.1652C>A
NR_026702.2:n.690C>A
NM_001144951.2:c.*683C>A	NP_001138423.1:n.*683C>A