Canonical Allele Identifier: CA353075398

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52292725-G-A
• MyVariant Identifiers: chr3:g.52326741G>A (hg19) ; chr3:g.52292725G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292725G>A , CM000665.2:g.52292725G>A	GRCh38
NC_000003.11:g.52326741G>A , CM000665.1:g.52326741G>A	GRCh37
NC_000003.10:g.52301781G>A	NCBI36
NG_023246.1:g.9906G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1171G>A MANE Select	ENSP00000389175.2:p.Ala391Thr
ENST00000305690.12:c.*290G>A	ENSP00000301965.9:n.*290G>A
ENST00000436784.6:c.1171G>A	ENSP00000389175.2:p.Ala391Thr
ENST00000461183.5:c.763+156G>A	ENSP00000417264.1:n.763+156G>A
ENST00000471180.5:c.634+156G>A	ENSP00000417526.1:n.634+156G>A
ENST00000473032.5:c.530-321G>A	ENSP00000418951.1:n.530-321G>A
ENST00000477382.1:c.*290G>A	ENSP00000419008.1:n.*290G>A
ENST00000486393.5:c.*534G>A	ENSP00000419868.1:n.*534G>A
ENST00000489173.1:n.1465G>A
NM_001144951.1:c.*290G>A	NP_001138423.1:n.*290G>A
NM_145262.3:c.1171G>A	NP_660305.2:p.Ala391Thr
NR_026699.1:n.1269G>A
NR_026700.1:n.695+156G>A
NR_026701.1:n.1267G>A
NR_026702.1:n.626-321G>A
XM_005264878.2:c.*290G>A	XP_005264935.1:n.*290G>A
XR_245095.2:n.2742+156G>A
XM_017005730.1:c.790G>A	XP_016861219.1:p.Ala264Thr
XM_024453351.1:c.1171G>A	XP_024309119.1:p.Ala391Thr
XM_024453352.1:c.*290G>A	XP_024309120.1:n.*290G>A
XR_001740022.2:n.3073G>A
XR_001740023.2:n.2917+156G>A
XR_245095.4:n.2743+156G>A
NM_145262.4:c.1171G>A MANE Select	NP_660305.2:p.Ala391Thr
NR_026699.2:n.1261G>A
NR_026700.2:n.687+156G>A
NR_026701.2:n.1259G>A
NR_026702.2:n.618-321G>A
NM_001144951.2:c.*290G>A	NP_001138423.1:n.*290G>A