Canonical Allele Identifier: CA353076695

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293079-G-A
• COSMIC: COSM6443251
• MyVariant Identifiers: chr3:g.52327095G>A (hg19) ; chr3:g.52293079G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293079G>A , CM000665.2:g.52293079G>A	GRCh38
NC_000003.11:g.52327095G>A , CM000665.1:g.52327095G>A	GRCh37
NC_000003.10:g.52302135G>A	NCBI36
NG_023246.1:g.10260G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1525G>A MANE Select	ENSP00000389175.2:p.Gly509Ser
ENST00000436784.6:c.1525G>A	ENSP00000389175.2:p.Gly509Ser
ENST00000461183.5:c.797G>A	ENSP00000417264.1:p.Arg266Lys
ENST00000471180.5:c.668G>A	ENSP00000417526.1:p.Arg223Lys
ENST00000473032.5:c.563G>A	ENSP00000418951.1:p.Arg188Lys
ENST00000486393.5:c.*888G>A	ENSP00000419868.1:n.*888G>A
ENST00000489173.1:n.1819G>A
NM_145262.3:c.1525G>A	NP_660305.2:p.Gly509Ser
NR_026699.1:n.1623G>A
NR_026700.1:n.729G>A
NR_026701.1:n.1621G>A
NR_026702.1:n.659G>A
XM_005264878.2:c.*644G>A	XP_005264935.1:n.*644G>A
XR_245095.2:n.2776G>A
XM_017005730.1:c.1144G>A	XP_016861219.1:p.Gly382Ser
XM_024453351.1:c.1525G>A	XP_024309119.1:p.Gly509Ser
XM_024453352.1:c.*644G>A	XP_024309120.1:n.*644G>A
XR_001740022.2:n.3427G>A
XR_001740023.2:n.2951G>A
XR_245095.4:n.2777G>A
NM_145262.4:c.1525G>A MANE Select	NP_660305.2:p.Gly509Ser
NR_026699.2:n.1615G>A
NR_026700.2:n.721G>A
NR_026701.2:n.1613G>A
NR_026702.2:n.651G>A
NM_001144951.2:c.*644G>A	NP_001138423.1:n.*644G>A