Canonical Allele Identifier: CA353076884

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327128C>G (hg19) ; chr3:g.52293112C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293112C>G , CM000665.2:g.52293112C>G	GRCh38
NC_000003.11:g.52327128C>G , CM000665.1:g.52327128C>G	GRCh37
NC_000003.10:g.52302168C>G	NCBI36
NG_023246.1:g.10293C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1558C>G MANE Select	ENSP00000389175.2:p.Leu520Val
ENST00000436784.6:c.1558C>G	ENSP00000389175.2:p.Leu520Val
ENST00000461183.5:c.830C>G	ENSP00000417264.1:p.Pro277Arg
ENST00000471180.5:c.701C>G	ENSP00000417526.1:p.Pro234Arg
ENST00000473032.5:c.596C>G	ENSP00000418951.1:p.Pro199Arg
ENST00000486393.5:c.*921C>G	ENSP00000419868.1:n.*921C>G
ENST00000489173.1:n.1852C>G
NM_145262.3:c.1558C>G	NP_660305.2:p.Leu520Val
NR_026699.1:n.1656C>G
NR_026700.1:n.762C>G
NR_026701.1:n.1654C>G
NR_026702.1:n.692C>G
XM_005264878.2:c.*677C>G	XP_005264935.1:n.*677C>G
XR_245095.2:n.2809C>G
XM_017005730.1:c.1177C>G	XP_016861219.1:p.Leu393Val
XM_024453351.1:c.1558C>G	XP_024309119.1:p.Leu520Val
XM_024453352.1:c.*677C>G	XP_024309120.1:n.*677C>G
XR_001740022.2:n.3460C>G
XR_001740023.2:n.2984C>G
XR_245095.4:n.2810C>G
NM_145262.4:c.1558C>G MANE Select	NP_660305.2:p.Leu520Val
NR_026699.2:n.1648C>G
NR_026700.2:n.754C>G
NR_026701.2:n.1646C>G
NR_026702.2:n.684C>G
NM_001144951.2:c.*677C>G	NP_001138423.1:n.*677C>G