Canonical Allele Identifier: CA353076902

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327131C>G (hg19) ; chr3:g.52293115C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293115C>G , CM000665.2:g.52293115C>G	GRCh38
NC_000003.11:g.52327131C>G , CM000665.1:g.52327131C>G	GRCh37
NC_000003.10:g.52302171C>G	NCBI36
NG_023246.1:g.10296C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1561C>G MANE Select	ENSP00000389175.2:p.Arg521Gly
ENST00000436784.6:c.1561C>G	ENSP00000389175.2:p.Arg521Gly
ENST00000461183.5:c.833C>G	ENSP00000417264.1:p.Ala278Gly
ENST00000471180.5:c.704C>G	ENSP00000417526.1:p.Ala235Gly
ENST00000473032.5:c.599C>G	ENSP00000418951.1:p.Ala200Gly
ENST00000486393.5:c.*924C>G	ENSP00000419868.1:n.*924C>G
ENST00000489173.1:n.1855C>G
NM_145262.3:c.1561C>G	NP_660305.2:p.Arg521Gly
NR_026699.1:n.1659C>G
NR_026700.1:n.765C>G
NR_026701.1:n.1657C>G
NR_026702.1:n.695C>G
XM_005264878.2:c.*680C>G	XP_005264935.1:n.*680C>G
XR_245095.2:n.2812C>G
XM_017005730.1:c.1180C>G	XP_016861219.1:p.Arg394Gly
XM_024453351.1:c.1561C>G	XP_024309119.1:p.Arg521Gly
XM_024453352.1:c.*680C>G	XP_024309120.1:n.*680C>G
XR_001740022.2:n.3463C>G
XR_001740023.2:n.2987C>G
XR_245095.4:n.2813C>G
NM_145262.4:c.1561C>G MANE Select	NP_660305.2:p.Arg521Gly
NR_026699.2:n.1651C>G
NR_026700.2:n.757C>G
NR_026701.2:n.1649C>G
NR_026702.2:n.687C>G
NM_001144951.2:c.*680C>G	NP_001138423.1:n.*680C>G