Canonical Allele Identifier: CA353076435

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327040T>G (hg19) ; chr3:g.52293024T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293024T>G , CM000665.2:g.52293024T>G	GRCh38
NC_000003.11:g.52327040T>G , CM000665.1:g.52327040T>G	GRCh37
NC_000003.10:g.52302080T>G	NCBI36
NG_023246.1:g.10205T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1470T>G MANE Select	ENSP00000389175.2:p.His490Gln
ENST00000436784.6:c.1470T>G	ENSP00000389175.2:p.His490Gln
ENST00000461183.5:c.764-22T>G	ENSP00000417264.1:n.764-22T>G
ENST00000471180.5:c.635-22T>G	ENSP00000417526.1:n.635-22T>G
ENST00000473032.5:c.530-22T>G	ENSP00000418951.1:n.530-22T>G
ENST00000486393.5:c.*833T>G	ENSP00000419868.1:n.*833T>G
ENST00000489173.1:n.1764T>G
NM_145262.3:c.1470T>G	NP_660305.2:p.His490Gln
NR_026699.1:n.1568T>G
NR_026700.1:n.696-22T>G
NR_026701.1:n.1566T>G
NR_026702.1:n.626-22T>G
XM_005264878.2:c.*589T>G	XP_005264935.1:n.*589T>G
XR_245095.2:n.2743-22T>G
XM_017005730.1:c.1089T>G	XP_016861219.1:p.His363Gln
XM_024453351.1:c.1470T>G	XP_024309119.1:p.His490Gln
XM_024453352.1:c.*589T>G	XP_024309120.1:n.*589T>G
XR_001740022.2:n.3372T>G
XR_001740023.2:n.2918-22T>G
XR_245095.4:n.2744-22T>G
NM_145262.4:c.1470T>G MANE Select	NP_660305.2:p.His490Gln
NR_026699.2:n.1560T>G
NR_026700.2:n.688-22T>G
NR_026701.2:n.1558T>G
NR_026702.2:n.618-22T>G
NM_001144951.2:c.*589T>G	NP_001138423.1:n.*589T>G