Canonical Allele Identifier: CA353076692

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293078-A-T
• MyVariant Identifiers: chr3:g.52327094A>T (hg19) ; chr3:g.52293078A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293078A>T , CM000665.2:g.52293078A>T	GRCh38
NC_000003.11:g.52327094A>T , CM000665.1:g.52327094A>T	GRCh37
NC_000003.10:g.52302134A>T	NCBI36
NG_023246.1:g.10259A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1524A>T MANE Select	ENSP00000389175.2:p.Thr508=
ENST00000436784.6:c.1524A>T	ENSP00000389175.2:p.Thr508=
ENST00000461183.5:c.796A>T	ENSP00000417264.1:p.Arg266Trp
ENST00000471180.5:c.667A>T	ENSP00000417526.1:p.Arg223Trp
ENST00000473032.5:c.562A>T	ENSP00000418951.1:p.Arg188Trp
ENST00000486393.5:c.*887A>T	ENSP00000419868.1:n.*887A>T
ENST00000489173.1:n.1818A>T
NM_145262.3:c.1524A>T	NP_660305.2:p.Thr508=
NR_026699.1:n.1622A>T
NR_026700.1:n.728A>T
NR_026701.1:n.1620A>T
NR_026702.1:n.658A>T
XM_005264878.2:c.*643A>T	XP_005264935.1:n.*643A>T
XR_245095.2:n.2775A>T
XM_017005730.1:c.1143A>T	XP_016861219.1:p.Thr381=
XM_024453351.1:c.1524A>T	XP_024309119.1:p.Thr508=
XM_024453352.1:c.*643A>T	XP_024309120.1:n.*643A>T
XR_001740022.2:n.3426A>T
XR_001740023.2:n.2950A>T
XR_245095.4:n.2776A>T
NM_145262.4:c.1524A>T MANE Select	NP_660305.2:p.Thr508=
NR_026699.2:n.1614A>T
NR_026700.2:n.720A>T
NR_026701.2:n.1612A>T
NR_026702.2:n.650A>T
NM_001144951.2:c.*643A>T	NP_001138423.1:n.*643A>T