Canonical Allele Identifier: CA353076127

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326973A>G (hg19) ; chr3:g.52292957A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292957A>G , CM000665.2:g.52292957A>G	GRCh38
NC_000003.11:g.52326973A>G , CM000665.1:g.52326973A>G	GRCh37
NC_000003.10:g.52302013A>G	NCBI36
NG_023246.1:g.10138A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1403A>G MANE Select	ENSP00000389175.2:p.Glu468Gly
ENST00000305690.12:c.*522A>G	ENSP00000301965.9:n.*522A>G
ENST00000436784.6:c.1403A>G	ENSP00000389175.2:p.Glu468Gly
ENST00000461183.5:c.764-89A>G	ENSP00000417264.1:n.764-89A>G
ENST00000471180.5:c.635-89A>G	ENSP00000417526.1:n.635-89A>G
ENST00000473032.5:c.530-89A>G	ENSP00000418951.1:n.530-89A>G
ENST00000477382.1:c.*522A>G	ENSP00000419008.1:n.*522A>G
ENST00000486393.5:c.*766A>G	ENSP00000419868.1:n.*766A>G
ENST00000489173.1:n.1697A>G
NM_001144951.1:c.*522A>G	NP_001138423.1:n.*522A>G
NM_145262.3:c.1403A>G	NP_660305.2:p.Glu468Gly
NR_026699.1:n.1501A>G
NR_026700.1:n.696-89A>G
NR_026701.1:n.1499A>G
NR_026702.1:n.626-89A>G
XM_005264878.2:c.*522A>G	XP_005264935.1:n.*522A>G
XR_245095.2:n.2743-89A>G
XM_017005730.1:c.1022A>G	XP_016861219.1:p.Glu341Gly
XM_024453351.1:c.1403A>G	XP_024309119.1:p.Glu468Gly
XM_024453352.1:c.*522A>G	XP_024309120.1:n.*522A>G
XR_001740022.2:n.3305A>G
XR_001740023.2:n.2918-89A>G
XR_245095.4:n.2744-89A>G
NM_145262.4:c.1403A>G MANE Select	NP_660305.2:p.Glu468Gly
NR_026699.2:n.1493A>G
NR_026700.2:n.688-89A>G
NR_026701.2:n.1491A>G
NR_026702.2:n.618-89A>G
NM_001144951.2:c.*522A>G	NP_001138423.1:n.*522A>G