Canonical Allele Identifier: CA353076610

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327076G>A (hg19) ; chr3:g.52293060G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293060G>A , CM000665.2:g.52293060G>A	GRCh38
NC_000003.11:g.52327076G>A , CM000665.1:g.52327076G>A	GRCh37
NC_000003.10:g.52302116G>A	NCBI36
NG_023246.1:g.10241G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1506G>A MANE Select	ENSP00000389175.2:p.Leu502=
ENST00000436784.6:c.1506G>A	ENSP00000389175.2:p.Leu502=
ENST00000461183.5:c.778G>A	ENSP00000417264.1:p.Ala260Thr
ENST00000471180.5:c.649G>A	ENSP00000417526.1:p.Ala217Thr
ENST00000473032.5:c.544G>A	ENSP00000418951.1:p.Ala182Thr
ENST00000486393.5:c.*869G>A	ENSP00000419868.1:n.*869G>A
ENST00000489173.1:n.1800G>A
NM_145262.3:c.1506G>A	NP_660305.2:p.Leu502=
NR_026699.1:n.1604G>A
NR_026700.1:n.710G>A
NR_026701.1:n.1602G>A
NR_026702.1:n.640G>A
XM_005264878.2:c.*625G>A	XP_005264935.1:n.*625G>A
XR_245095.2:n.2757G>A
XM_017005730.1:c.1125G>A	XP_016861219.1:p.Leu375=
XM_024453351.1:c.1506G>A	XP_024309119.1:p.Leu502=
XM_024453352.1:c.*625G>A	XP_024309120.1:n.*625G>A
XR_001740022.2:n.3408G>A
XR_001740023.2:n.2932G>A
XR_245095.4:n.2758G>A
NM_145262.4:c.1506G>A MANE Select	NP_660305.2:p.Leu502=
NR_026699.2:n.1596G>A
NR_026700.2:n.702G>A
NR_026701.2:n.1594G>A
NR_026702.2:n.632G>A
NM_001144951.2:c.*625G>A	NP_001138423.1:n.*625G>A