Canonical Allele Identifier: CA353076609

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327075T>G (hg19) ; chr3:g.52293059T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293059T>G , CM000665.2:g.52293059T>G	GRCh38
NC_000003.11:g.52327075T>G , CM000665.1:g.52327075T>G	GRCh37
NC_000003.10:g.52302115T>G	NCBI36
NG_023246.1:g.10240T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1505T>G MANE Select	ENSP00000389175.2:p.Leu502Arg
ENST00000436784.6:c.1505T>G	ENSP00000389175.2:p.Leu502Arg
ENST00000461183.5:c.777T>G	ENSP00000417264.1:p.Pro259=
ENST00000471180.5:c.648T>G	ENSP00000417526.1:p.Pro216=
ENST00000473032.5:c.543T>G	ENSP00000418951.1:p.Pro181=
ENST00000486393.5:c.*868T>G	ENSP00000419868.1:n.*868T>G
ENST00000489173.1:n.1799T>G
NM_145262.3:c.1505T>G	NP_660305.2:p.Leu502Arg
NR_026699.1:n.1603T>G
NR_026700.1:n.709T>G
NR_026701.1:n.1601T>G
NR_026702.1:n.639T>G
XM_005264878.2:c.*624T>G	XP_005264935.1:n.*624T>G
XR_245095.2:n.2756T>G
XM_017005730.1:c.1124T>G	XP_016861219.1:p.Leu375Arg
XM_024453351.1:c.1505T>G	XP_024309119.1:p.Leu502Arg
XM_024453352.1:c.*624T>G	XP_024309120.1:n.*624T>G
XR_001740022.2:n.3407T>G
XR_001740023.2:n.2931T>G
XR_245095.4:n.2757T>G
NM_145262.4:c.1505T>G MANE Select	NP_660305.2:p.Leu502Arg
NR_026699.2:n.1595T>G
NR_026700.2:n.701T>G
NR_026701.2:n.1593T>G
NR_026702.2:n.631T>G
NM_001144951.2:c.*624T>G	NP_001138423.1:n.*624T>G