Canonical Allele Identifier: CA353076668

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327090T>A (hg19) ; chr3:g.52293074T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293074T>A , CM000665.2:g.52293074T>A	GRCh38
NC_000003.11:g.52327090T>A , CM000665.1:g.52327090T>A	GRCh37
NC_000003.10:g.52302130T>A	NCBI36
NG_023246.1:g.10255T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1520T>A MANE Select	ENSP00000389175.2:p.Met507Lys
ENST00000436784.6:c.1520T>A	ENSP00000389175.2:p.Met507Lys
ENST00000461183.5:c.792T>A	ENSP00000417264.1:p.Asp264Glu
ENST00000471180.5:c.663T>A	ENSP00000417526.1:p.Asp221Glu
ENST00000473032.5:c.558T>A	ENSP00000418951.1:p.Asp186Glu
ENST00000486393.5:c.*883T>A	ENSP00000419868.1:n.*883T>A
ENST00000489173.1:n.1814T>A
NM_145262.3:c.1520T>A	NP_660305.2:p.Met507Lys
NR_026699.1:n.1618T>A
NR_026700.1:n.724T>A
NR_026701.1:n.1616T>A
NR_026702.1:n.654T>A
XM_005264878.2:c.*639T>A	XP_005264935.1:n.*639T>A
XR_245095.2:n.2771T>A
XM_017005730.1:c.1139T>A	XP_016861219.1:p.Met380Lys
XM_024453351.1:c.1520T>A	XP_024309119.1:p.Met507Lys
XM_024453352.1:c.*639T>A	XP_024309120.1:n.*639T>A
XR_001740022.2:n.3422T>A
XR_001740023.2:n.2946T>A
XR_245095.4:n.2772T>A
NM_145262.4:c.1520T>A MANE Select	NP_660305.2:p.Met507Lys
NR_026699.2:n.1610T>A
NR_026700.2:n.716T>A
NR_026701.2:n.1608T>A
NR_026702.2:n.646T>A
NM_001144951.2:c.*639T>A	NP_001138423.1:n.*639T>A