Canonical Allele Identifier: CA433882943

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326953T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292937T>A , CM000665.2:g.52292937T>A	GRCh38
NC_000003.11:g.52326953T>A , CM000665.1:g.52326953T>A	GRCh37
NC_000003.10:g.52301993T>A	NCBI36
NG_023246.1:g.10118T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1383T>A MANE Select	ENSP00000389175.2:p.Ala461=
ENST00000305690.12:c.*502T>A	ENSP00000301965.9:n.*502T>A
ENST00000436784.6:c.1383T>A	ENSP00000389175.2:p.Ala461=
ENST00000461183.5:c.764-109T>A	ENSP00000417264.1:n.764-109T>A
ENST00000471180.5:c.635-109T>A	ENSP00000417526.1:n.635-109T>A
ENST00000473032.5:c.530-109T>A	ENSP00000418951.1:n.530-109T>A
ENST00000477382.1:c.*502T>A	ENSP00000419008.1:n.*502T>A
ENST00000486393.5:c.*746T>A	ENSP00000419868.1:n.*746T>A
ENST00000489173.1:n.1677T>A
NM_001144951.1:c.*502T>A	NP_001138423.1:n.*502T>A
NM_145262.3:c.1383T>A	NP_660305.2:p.Ala461=
NR_026699.1:n.1481T>A
NR_026700.1:n.696-109T>A
NR_026701.1:n.1479T>A
NR_026702.1:n.626-109T>A
XM_005264878.2:c.*502T>A	XP_005264935.1:n.*502T>A
XR_245095.2:n.2743-109T>A
XM_017005730.1:c.1002T>A	XP_016861219.1:p.Ala334=
XM_024453351.1:c.1383T>A	XP_024309119.1:p.Ala461=
XM_024453352.1:c.*502T>A	XP_024309120.1:n.*502T>A
XR_001740022.2:n.3285T>A
XR_001740023.2:n.2918-109T>A
XR_245095.4:n.2744-109T>A
NM_145262.4:c.1383T>A MANE Select	NP_660305.2:p.Ala461=
NR_026699.2:n.1473T>A
NR_026700.2:n.688-109T>A
NR_026701.2:n.1471T>A
NR_026702.2:n.618-109T>A
NM_001144951.2:c.*502T>A	NP_001138423.1:n.*502T>A