Canonical Allele Identifier: CA353076711

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1361727882
• gnomAD v3: 3-52293082-A-G
• gnomAD v4: 3-52293082-A-G
• MyVariant Identifiers: chr3:g.52327098A>G (hg19) ; chr3:g.52293082A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293082A>G , CM000665.2:g.52293082A>G	GRCh38
NC_000003.11:g.52327098A>G , CM000665.1:g.52327098A>G	GRCh37
NC_000003.10:g.52302138A>G	NCBI36
NG_023246.1:g.10263A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1528A>G MANE Select	ENSP00000389175.2:p.Thr510Ala
ENST00000436784.6:c.1528A>G	ENSP00000389175.2:p.Thr510Ala
ENST00000461183.5:c.800A>G	ENSP00000417264.1:p.Tyr267Cys
ENST00000471180.5:c.671A>G	ENSP00000417526.1:p.Tyr224Cys
ENST00000473032.5:c.566A>G	ENSP00000418951.1:p.Tyr189Cys
ENST00000486393.5:c.*891A>G	ENSP00000419868.1:n.*891A>G
ENST00000489173.1:n.1822A>G
NM_145262.3:c.1528A>G	NP_660305.2:p.Thr510Ala
NR_026699.1:n.1626A>G
NR_026700.1:n.732A>G
NR_026701.1:n.1624A>G
NR_026702.1:n.662A>G
XM_005264878.2:c.*647A>G	XP_005264935.1:n.*647A>G
XR_245095.2:n.2779A>G
XM_017005730.1:c.1147A>G	XP_016861219.1:p.Thr383Ala
XM_024453351.1:c.1528A>G	XP_024309119.1:p.Thr510Ala
XM_024453352.1:c.*647A>G	XP_024309120.1:n.*647A>G
XR_001740022.2:n.3430A>G
XR_001740023.2:n.2954A>G
XR_245095.4:n.2780A>G
NM_145262.4:c.1528A>G MANE Select	NP_660305.2:p.Thr510Ala
NR_026699.2:n.1618A>G
NR_026700.2:n.724A>G
NR_026701.2:n.1616A>G
NR_026702.2:n.654A>G
NM_001144951.2:c.*647A>G	NP_001138423.1:n.*647A>G