Canonical Allele Identifier: CA353076685

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327093C>G (hg19) ; chr3:g.52293077C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293077C>G , CM000665.2:g.52293077C>G	GRCh38
NC_000003.11:g.52327093C>G , CM000665.1:g.52327093C>G	GRCh37
NC_000003.10:g.52302133C>G	NCBI36
NG_023246.1:g.10258C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1523C>G MANE Select	ENSP00000389175.2:p.Thr508Arg
ENST00000436784.6:c.1523C>G	ENSP00000389175.2:p.Thr508Arg
ENST00000461183.5:c.795C>G	ENSP00000417264.1:p.Asp265Glu
ENST00000471180.5:c.666C>G	ENSP00000417526.1:p.Asp222Glu
ENST00000473032.5:c.561C>G	ENSP00000418951.1:p.Asp187Glu
ENST00000486393.5:c.*886C>G	ENSP00000419868.1:n.*886C>G
ENST00000489173.1:n.1817C>G
NM_145262.3:c.1523C>G	NP_660305.2:p.Thr508Arg
NR_026699.1:n.1621C>G
NR_026700.1:n.727C>G
NR_026701.1:n.1619C>G
NR_026702.1:n.657C>G
XM_005264878.2:c.*642C>G	XP_005264935.1:n.*642C>G
XR_245095.2:n.2774C>G
XM_017005730.1:c.1142C>G	XP_016861219.1:p.Thr381Arg
XM_024453351.1:c.1523C>G	XP_024309119.1:p.Thr508Arg
XM_024453352.1:c.*642C>G	XP_024309120.1:n.*642C>G
XR_001740022.2:n.3425C>G
XR_001740023.2:n.2949C>G
XR_245095.4:n.2775C>G
NM_145262.4:c.1523C>G MANE Select	NP_660305.2:p.Thr508Arg
NR_026699.2:n.1613C>G
NR_026700.2:n.719C>G
NR_026701.2:n.1611C>G
NR_026702.2:n.649C>G
NM_001144951.2:c.*642C>G	NP_001138423.1:n.*642C>G