Canonical Allele Identifier: CA2432237

Gene: GLYCTK

Linked Data

• dbSNP Id: rs781660673
• ExAC: 3:52326600 A / G
• gnomAD v2: 3-52326600-A-G
• gnomAD v3: 3-52292584-A-G
• gnomAD v4: 3-52292584-A-G
• MyVariant Identifiers: chr3:g.52326600A>G (hg19) ; chr3:g.52292584A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292584A>G , CM000665.2:g.52292584A>G	GRCh38
NC_000003.11:g.52326600A>G , CM000665.1:g.52326600A>G	GRCh37
NC_000003.10:g.52301640A>G	NCBI36
NG_023246.1:g.9765A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1030A>G MANE Select	ENSP00000389175.2:p.Met344Val
ENST00000305690.12:c.*149A>G	ENSP00000301965.9:n.*149A>G
ENST00000436784.6:c.1030A>G	ENSP00000389175.2:p.Met344Val
ENST00000461183.5:c.763+15A>G	ENSP00000417264.1:n.763+15A>G
ENST00000471180.5:c.634+15A>G	ENSP00000417526.1:n.634+15A>G
ENST00000473032.5:c.530-462A>G	ENSP00000418951.1:n.530-462A>G
ENST00000477382.1:c.*149A>G	ENSP00000419008.1:n.*149A>G
ENST00000486393.5:c.*393A>G	ENSP00000419868.1:n.*393A>G
ENST00000489173.1:n.1324A>G
NM_001144951.1:c.*149A>G	NP_001138423.1:n.*149A>G
NM_145262.3:c.1030A>G	NP_660305.2:p.Met344Val
NR_026699.1:n.1128A>G
NR_026700.1:n.695+15A>G
NR_026701.1:n.1126A>G
NR_026702.1:n.626-462A>G
XM_005264878.2:c.*149A>G	XP_005264935.1:n.*149A>G
XR_245095.2:n.2742+15A>G
XM_017005730.1:c.649A>G	XP_016861219.1:p.Met217Val
XM_024453351.1:c.1030A>G	XP_024309119.1:p.Met344Val
XM_024453352.1:c.*149A>G	XP_024309120.1:n.*149A>G
XR_001740022.2:n.2932A>G
XR_001740023.2:n.2917+15A>G
XR_245095.4:n.2743+15A>G
NM_145262.4:c.1030A>G MANE Select	NP_660305.2:p.Met344Val
NR_026699.2:n.1120A>G
NR_026700.2:n.687+15A>G
NR_026701.2:n.1118A>G
NR_026702.2:n.618-462A>G
NM_001144951.2:c.*149A>G	NP_001138423.1:n.*149A>G