Canonical Allele Identifier: CA543056261

Gene: GLYCTK

Linked Data

• dbSNP Id: rs934273983
• gnomAD v2: 3-52327346-C-T
• gnomAD v3: 3-52293330-C-T
• gnomAD v4: 3-52293330-C-T
• MyVariant Identifiers: chr3:g.52327346C>T (hg19) ; chr3:g.52293330C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293330C>T , CM000665.2:g.52293330C>T	GRCh38
NC_000003.11:g.52327346C>T , CM000665.1:g.52327346C>T	GRCh37
NC_000003.10:g.52302386C>T	NCBI36
NG_023246.1:g.10511C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*204C>T MANE Select	ENSP00000389175.2:n.*204C>T
ENST00000436784.6:c.*204C>T	ENSP00000389175.2:n.*204C>T
ENST00000471180.5:c.*82C>T	ENSP00000417526.1:n.*82C>T
ENST00000473032.5:c.*82C>T	ENSP00000418951.1:n.*82C>T
ENST00000486393.5:c.*1139C>T	ENSP00000419868.1:n.*1139C>T
ENST00000489173.1:n.1938C>T
NM_145262.3:c.*204C>T	NP_660305.2:n.*204C>T
NR_026699.1:n.1874C>T
NR_026700.1:n.866C>T
NR_026701.1:n.1758C>T
NR_026702.1:n.796C>T
XM_005264878.2:c.*895C>T	XP_005264935.1:n.*895C>T
XR_245095.2:n.2913C>T
XM_017005730.1:c.*204C>T	XP_016861219.1:n.*204C>T
XM_024453351.1:c.*204C>T	XP_024309119.1:n.*204C>T
XM_024453352.1:c.*895C>T	XP_024309120.1:n.*895C>T
XR_001740022.2:n.3564C>T
XR_001740023.2:n.3088C>T
XR_245095.4:n.2914C>T
NM_145262.4:c.*204C>T MANE Select	NP_660305.2:n.*204C>T
NR_026699.2:n.1866C>T
NR_026700.2:n.858C>T
NR_026701.2:n.1750C>T
NR_026702.2:n.788C>T
NM_001144951.2:c.*895C>T	NP_001138423.1:n.*895C>T