Canonical Allele Identifier: CA353076621

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293064-C-T
• MyVariant Identifiers: chr3:g.52327080C>T (hg19) ; chr3:g.52293064C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293064C>T , CM000665.2:g.52293064C>T	GRCh38
NC_000003.11:g.52327080C>T , CM000665.1:g.52327080C>T	GRCh37
NC_000003.10:g.52302120C>T	NCBI36
NG_023246.1:g.10245C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1510C>T MANE Select	ENSP00000389175.2:p.His504Tyr
ENST00000436784.6:c.1510C>T	ENSP00000389175.2:p.His504Tyr
ENST00000461183.5:c.782C>T	ENSP00000417264.1:p.Ala261Val
ENST00000471180.5:c.653C>T	ENSP00000417526.1:p.Ala218Val
ENST00000473032.5:c.548C>T	ENSP00000418951.1:p.Ala183Val
ENST00000486393.5:c.*873C>T	ENSP00000419868.1:n.*873C>T
ENST00000489173.1:n.1804C>T
NM_145262.3:c.1510C>T	NP_660305.2:p.His504Tyr
NR_026699.1:n.1608C>T
NR_026700.1:n.714C>T
NR_026701.1:n.1606C>T
NR_026702.1:n.644C>T
XM_005264878.2:c.*629C>T	XP_005264935.1:n.*629C>T
XR_245095.2:n.2761C>T
XM_017005730.1:c.1129C>T	XP_016861219.1:p.His377Tyr
XM_024453351.1:c.1510C>T	XP_024309119.1:p.His504Tyr
XM_024453352.1:c.*629C>T	XP_024309120.1:n.*629C>T
XR_001740022.2:n.3412C>T
XR_001740023.2:n.2936C>T
XR_245095.4:n.2762C>T
NM_145262.4:c.1510C>T MANE Select	NP_660305.2:p.His504Tyr
NR_026699.2:n.1600C>T
NR_026700.2:n.706C>T
NR_026701.2:n.1598C>T
NR_026702.2:n.636C>T
NM_001144951.2:c.*629C>T	NP_001138423.1:n.*629C>T