Canonical Allele Identifier: CA353076292

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327012C>T (hg19) ; chr3:g.52292996C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292996C>T , CM000665.2:g.52292996C>T	GRCh38
NC_000003.11:g.52327012C>T , CM000665.1:g.52327012C>T	GRCh37
NC_000003.10:g.52302052C>T	NCBI36
NG_023246.1:g.10177C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1442C>T MANE Select	ENSP00000389175.2:p.Ala481Val
ENST00000305690.12:c.*561C>T	ENSP00000301965.9:n.*561C>T
ENST00000436784.6:c.1442C>T	ENSP00000389175.2:p.Ala481Val
ENST00000461183.5:c.764-50C>T	ENSP00000417264.1:n.764-50C>T
ENST00000471180.5:c.635-50C>T	ENSP00000417526.1:n.635-50C>T
ENST00000473032.5:c.530-50C>T	ENSP00000418951.1:n.530-50C>T
ENST00000477382.1:c.*561C>T	ENSP00000419008.1:n.*561C>T
ENST00000486393.5:c.*805C>T	ENSP00000419868.1:n.*805C>T
ENST00000489173.1:n.1736C>T
NM_001144951.1:c.*561C>T	NP_001138423.1:n.*561C>T
NM_145262.3:c.1442C>T	NP_660305.2:p.Ala481Val
NR_026699.1:n.1540C>T
NR_026700.1:n.696-50C>T
NR_026701.1:n.1538C>T
NR_026702.1:n.626-50C>T
XM_005264878.2:c.*561C>T	XP_005264935.1:n.*561C>T
XR_245095.2:n.2743-50C>T
XM_017005730.1:c.1061C>T	XP_016861219.1:p.Ala354Val
XM_024453351.1:c.1442C>T	XP_024309119.1:p.Ala481Val
XM_024453352.1:c.*561C>T	XP_024309120.1:n.*561C>T
XR_001740022.2:n.3344C>T
XR_001740023.2:n.2918-50C>T
XR_245095.4:n.2744-50C>T
NM_145262.4:c.1442C>T MANE Select	NP_660305.2:p.Ala481Val
NR_026699.2:n.1532C>T
NR_026700.2:n.688-50C>T
NR_026701.2:n.1530C>T
NR_026702.2:n.618-50C>T
NM_001144951.2:c.*561C>T	NP_001138423.1:n.*561C>T