Canonical Allele Identifier: CA353075795

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52292878-A-G
• MyVariant Identifiers: chr3:g.52326894A>G (hg19) ; chr3:g.52292878A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292878A>G , CM000665.2:g.52292878A>G	GRCh38
NC_000003.11:g.52326894A>G , CM000665.1:g.52326894A>G	GRCh37
NC_000003.10:g.52301934A>G	NCBI36
NG_023246.1:g.10059A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1324A>G MANE Select	ENSP00000389175.2:p.Ile442Val
ENST00000305690.12:c.*443A>G	ENSP00000301965.9:n.*443A>G
ENST00000436784.6:c.1324A>G	ENSP00000389175.2:p.Ile442Val
ENST00000461183.5:c.764-168A>G	ENSP00000417264.1:n.764-168A>G
ENST00000471180.5:c.635-168A>G	ENSP00000417526.1:n.635-168A>G
ENST00000473032.5:c.530-168A>G	ENSP00000418951.1:n.530-168A>G
ENST00000477382.1:c.*443A>G	ENSP00000419008.1:n.*443A>G
ENST00000486393.5:c.*687A>G	ENSP00000419868.1:n.*687A>G
ENST00000489173.1:n.1618A>G
NM_001144951.1:c.*443A>G	NP_001138423.1:n.*443A>G
NM_145262.3:c.1324A>G	NP_660305.2:p.Ile442Val
NR_026699.1:n.1422A>G
NR_026700.1:n.696-168A>G
NR_026701.1:n.1420A>G
NR_026702.1:n.626-168A>G
XM_005264878.2:c.*443A>G	XP_005264935.1:n.*443A>G
XR_245095.2:n.2743-168A>G
XM_017005730.1:c.943A>G	XP_016861219.1:p.Ile315Val
XM_024453351.1:c.1324A>G	XP_024309119.1:p.Ile442Val
XM_024453352.1:c.*443A>G	XP_024309120.1:n.*443A>G
XR_001740022.2:n.3226A>G
XR_001740023.2:n.2918-168A>G
XR_245095.4:n.2744-168A>G
NM_145262.4:c.1324A>G MANE Select	NP_660305.2:p.Ile442Val
NR_026699.2:n.1414A>G
NR_026700.2:n.688-168A>G
NR_026701.2:n.1412A>G
NR_026702.2:n.618-168A>G
NM_001144951.2:c.*443A>G	NP_001138423.1:n.*443A>G