Canonical Allele Identifier: CA353076744

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327105T>A (hg19) ; chr3:g.52293089T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293089T>A , CM000665.2:g.52293089T>A	GRCh38
NC_000003.11:g.52327105T>A , CM000665.1:g.52327105T>A	GRCh37
NC_000003.10:g.52302145T>A	NCBI36
NG_023246.1:g.10270T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1535T>A MANE Select	ENSP00000389175.2:p.Val512Asp
ENST00000436784.6:c.1535T>A	ENSP00000389175.2:p.Val512Asp
ENST00000461183.5:c.807T>A	ENSP00000417264.1:p.Cys269Ter
ENST00000471180.5:c.678T>A	ENSP00000417526.1:p.Cys226Ter
ENST00000473032.5:c.573T>A	ENSP00000418951.1:p.Cys191Ter
ENST00000486393.5:c.*898T>A	ENSP00000419868.1:n.*898T>A
ENST00000489173.1:n.1829T>A
NM_145262.3:c.1535T>A	NP_660305.2:p.Val512Asp
NR_026699.1:n.1633T>A
NR_026700.1:n.739T>A
NR_026701.1:n.1631T>A
NR_026702.1:n.669T>A
XM_005264878.2:c.*654T>A	XP_005264935.1:n.*654T>A
XR_245095.2:n.2786T>A
XM_017005730.1:c.1154T>A	XP_016861219.1:p.Val385Asp
XM_024453351.1:c.1535T>A	XP_024309119.1:p.Val512Asp
XM_024453352.1:c.*654T>A	XP_024309120.1:n.*654T>A
XR_001740022.2:n.3437T>A
XR_001740023.2:n.2961T>A
XR_245095.4:n.2787T>A
NM_145262.4:c.1535T>A MANE Select	NP_660305.2:p.Val512Asp
NR_026699.2:n.1625T>A
NR_026700.2:n.731T>A
NR_026701.2:n.1623T>A
NR_026702.2:n.661T>A
NM_001144951.2:c.*654T>A	NP_001138423.1:n.*654T>A