Canonical Allele Identifier: CA353076282

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52292995-G-A
• MyVariant Identifiers: chr3:g.52327011G>A (hg19) ; chr3:g.52292995G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292995G>A , CM000665.2:g.52292995G>A	GRCh38
NC_000003.11:g.52327011G>A , CM000665.1:g.52327011G>A	GRCh37
NC_000003.10:g.52302051G>A	NCBI36
NG_023246.1:g.10176G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1441G>A MANE Select	ENSP00000389175.2:p.Ala481Thr
ENST00000305690.12:c.*560G>A	ENSP00000301965.9:n.*560G>A
ENST00000436784.6:c.1441G>A	ENSP00000389175.2:p.Ala481Thr
ENST00000461183.5:c.764-51G>A	ENSP00000417264.1:n.764-51G>A
ENST00000471180.5:c.635-51G>A	ENSP00000417526.1:n.635-51G>A
ENST00000473032.5:c.530-51G>A	ENSP00000418951.1:n.530-51G>A
ENST00000477382.1:c.*560G>A	ENSP00000419008.1:n.*560G>A
ENST00000486393.5:c.*804G>A	ENSP00000419868.1:n.*804G>A
ENST00000489173.1:n.1735G>A
NM_001144951.1:c.*560G>A	NP_001138423.1:n.*560G>A
NM_145262.3:c.1441G>A	NP_660305.2:p.Ala481Thr
NR_026699.1:n.1539G>A
NR_026700.1:n.696-51G>A
NR_026701.1:n.1537G>A
NR_026702.1:n.626-51G>A
XM_005264878.2:c.*560G>A	XP_005264935.1:n.*560G>A
XR_245095.2:n.2743-51G>A
XM_017005730.1:c.1060G>A	XP_016861219.1:p.Ala354Thr
XM_024453351.1:c.1441G>A	XP_024309119.1:p.Ala481Thr
XM_024453352.1:c.*560G>A	XP_024309120.1:n.*560G>A
XR_001740022.2:n.3343G>A
XR_001740023.2:n.2918-51G>A
XR_245095.4:n.2744-51G>A
NM_145262.4:c.1441G>A MANE Select	NP_660305.2:p.Ala481Thr
NR_026699.2:n.1531G>A
NR_026700.2:n.688-51G>A
NR_026701.2:n.1529G>A
NR_026702.2:n.618-51G>A
NM_001144951.2:c.*560G>A	NP_001138423.1:n.*560G>A