Canonical Allele Identifier: CA353076622

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327080C>G (hg19) ; chr3:g.52293064C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293064C>G , CM000665.2:g.52293064C>G	GRCh38
NC_000003.11:g.52327080C>G , CM000665.1:g.52327080C>G	GRCh37
NC_000003.10:g.52302120C>G	NCBI36
NG_023246.1:g.10245C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1510C>G MANE Select	ENSP00000389175.2:p.His504Asp
ENST00000436784.6:c.1510C>G	ENSP00000389175.2:p.His504Asp
ENST00000461183.5:c.782C>G	ENSP00000417264.1:p.Ala261Gly
ENST00000471180.5:c.653C>G	ENSP00000417526.1:p.Ala218Gly
ENST00000473032.5:c.548C>G	ENSP00000418951.1:p.Ala183Gly
ENST00000486393.5:c.*873C>G	ENSP00000419868.1:n.*873C>G
ENST00000489173.1:n.1804C>G
NM_145262.3:c.1510C>G	NP_660305.2:p.His504Asp
NR_026699.1:n.1608C>G
NR_026700.1:n.714C>G
NR_026701.1:n.1606C>G
NR_026702.1:n.644C>G
XM_005264878.2:c.*629C>G	XP_005264935.1:n.*629C>G
XR_245095.2:n.2761C>G
XM_017005730.1:c.1129C>G	XP_016861219.1:p.His377Asp
XM_024453351.1:c.1510C>G	XP_024309119.1:p.His504Asp
XM_024453352.1:c.*629C>G	XP_024309120.1:n.*629C>G
XR_001740022.2:n.3412C>G
XR_001740023.2:n.2936C>G
XR_245095.4:n.2762C>G
NM_145262.4:c.1510C>G MANE Select	NP_660305.2:p.His504Asp
NR_026699.2:n.1600C>G
NR_026700.2:n.706C>G
NR_026701.2:n.1598C>G
NR_026702.2:n.636C>G
NM_001144951.2:c.*629C>G	NP_001138423.1:n.*629C>G