Canonical Allele Identifier: CA353076888

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327129T>G (hg19) ; chr3:g.52293113T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293113T>G , CM000665.2:g.52293113T>G	GRCh38
NC_000003.11:g.52327129T>G , CM000665.1:g.52327129T>G	GRCh37
NC_000003.10:g.52302169T>G	NCBI36
NG_023246.1:g.10294T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1559T>G MANE Select	ENSP00000389175.2:p.Leu520Arg
ENST00000436784.6:c.1559T>G	ENSP00000389175.2:p.Leu520Arg
ENST00000461183.5:c.831T>G	ENSP00000417264.1:p.Pro277=
ENST00000471180.5:c.702T>G	ENSP00000417526.1:p.Pro234=
ENST00000473032.5:c.597T>G	ENSP00000418951.1:p.Pro199=
ENST00000486393.5:c.*922T>G	ENSP00000419868.1:n.*922T>G
ENST00000489173.1:n.1853T>G
NM_145262.3:c.1559T>G	NP_660305.2:p.Leu520Arg
NR_026699.1:n.1657T>G
NR_026700.1:n.763T>G
NR_026701.1:n.1655T>G
NR_026702.1:n.693T>G
XM_005264878.2:c.*678T>G	XP_005264935.1:n.*678T>G
XR_245095.2:n.2810T>G
XM_017005730.1:c.1178T>G	XP_016861219.1:p.Leu393Arg
XM_024453351.1:c.1559T>G	XP_024309119.1:p.Leu520Arg
XM_024453352.1:c.*678T>G	XP_024309120.1:n.*678T>G
XR_001740022.2:n.3461T>G
XR_001740023.2:n.2985T>G
XR_245095.4:n.2811T>G
NM_145262.4:c.1559T>G MANE Select	NP_660305.2:p.Leu520Arg
NR_026699.2:n.1649T>G
NR_026700.2:n.755T>G
NR_026701.2:n.1647T>G
NR_026702.2:n.685T>G
NM_001144951.2:c.*678T>G	NP_001138423.1:n.*678T>G