Canonical Allele Identifier: CA353076456

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327044T>G (hg19) ; chr3:g.52293028T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293028T>G , CM000665.2:g.52293028T>G	GRCh38
NC_000003.11:g.52327044T>G , CM000665.1:g.52327044T>G	GRCh37
NC_000003.10:g.52302084T>G	NCBI36
NG_023246.1:g.10209T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1474T>G MANE Select	ENSP00000389175.2:p.Phe492Val
ENST00000436784.6:c.1474T>G	ENSP00000389175.2:p.Phe492Val
ENST00000461183.5:c.764-18T>G	ENSP00000417264.1:n.764-18T>G
ENST00000471180.5:c.635-18T>G	ENSP00000417526.1:n.635-18T>G
ENST00000473032.5:c.530-18T>G	ENSP00000418951.1:n.530-18T>G
ENST00000486393.5:c.*837T>G	ENSP00000419868.1:n.*837T>G
ENST00000489173.1:n.1768T>G
NM_145262.3:c.1474T>G	NP_660305.2:p.Phe492Val
NR_026699.1:n.1572T>G
NR_026700.1:n.696-18T>G
NR_026701.1:n.1570T>G
NR_026702.1:n.626-18T>G
XM_005264878.2:c.*593T>G	XP_005264935.1:n.*593T>G
XR_245095.2:n.2743-18T>G
XM_017005730.1:c.1093T>G	XP_016861219.1:p.Phe365Val
XM_024453351.1:c.1474T>G	XP_024309119.1:p.Phe492Val
XM_024453352.1:c.*593T>G	XP_024309120.1:n.*593T>G
XR_001740022.2:n.3376T>G
XR_001740023.2:n.2918-18T>G
XR_245095.4:n.2744-18T>G
NM_145262.4:c.1474T>G MANE Select	NP_660305.2:p.Phe492Val
NR_026699.2:n.1564T>G
NR_026700.2:n.688-18T>G
NR_026701.2:n.1562T>G
NR_026702.2:n.618-18T>G
NM_001144951.2:c.*593T>G	NP_001138423.1:n.*593T>G