Canonical Allele Identifier: CA353076827

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327119C>G (hg19) ; chr3:g.52293103C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293103C>G , CM000665.2:g.52293103C>G	GRCh38
NC_000003.11:g.52327119C>G , CM000665.1:g.52327119C>G	GRCh37
NC_000003.10:g.52302159C>G	NCBI36
NG_023246.1:g.10284C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1549C>G MANE Select	ENSP00000389175.2:p.Leu517Val
ENST00000436784.6:c.1549C>G	ENSP00000389175.2:p.Leu517Val
ENST00000461183.5:c.821C>G	ENSP00000417264.1:p.Pro274Arg
ENST00000471180.5:c.692C>G	ENSP00000417526.1:p.Pro231Arg
ENST00000473032.5:c.587C>G	ENSP00000418951.1:p.Pro196Arg
ENST00000486393.5:c.*912C>G	ENSP00000419868.1:n.*912C>G
ENST00000489173.1:n.1843C>G
NM_145262.3:c.1549C>G	NP_660305.2:p.Leu517Val
NR_026699.1:n.1647C>G
NR_026700.1:n.753C>G
NR_026701.1:n.1645C>G
NR_026702.1:n.683C>G
XM_005264878.2:c.*668C>G	XP_005264935.1:n.*668C>G
XR_245095.2:n.2800C>G
XM_017005730.1:c.1168C>G	XP_016861219.1:p.Leu390Val
XM_024453351.1:c.1549C>G	XP_024309119.1:p.Leu517Val
XM_024453352.1:c.*668C>G	XP_024309120.1:n.*668C>G
XR_001740022.2:n.3451C>G
XR_001740023.2:n.2975C>G
XR_245095.4:n.2801C>G
NM_145262.4:c.1549C>G MANE Select	NP_660305.2:p.Leu517Val
NR_026699.2:n.1639C>G
NR_026700.2:n.745C>G
NR_026701.2:n.1637C>G
NR_026702.2:n.675C>G
NM_001144951.2:c.*668C>G	NP_001138423.1:n.*668C>G