Canonical Allele Identifier: CA353076548

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1385280333
• COSMIC: COSM5864972
• MyVariant Identifiers: chr3:g.52327063G>A (hg19) ; chr3:g.52293047G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293047G>A , CM000665.2:g.52293047G>A	GRCh38
NC_000003.11:g.52327063G>A , CM000665.1:g.52327063G>A	GRCh37
NC_000003.10:g.52302103G>A	NCBI36
NG_023246.1:g.10228G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1493G>A MANE Select	ENSP00000389175.2:p.Gly498Asp
ENST00000436784.6:c.1493G>A	ENSP00000389175.2:p.Gly498Asp
ENST00000461183.5:c.765G>A	ENSP00000417264.1:p.Gly255=
ENST00000471180.5:c.636G>A	ENSP00000417526.1:p.Gly212=
ENST00000473032.5:c.531G>A	ENSP00000418951.1:p.Gly177=
ENST00000486393.5:c.*856G>A	ENSP00000419868.1:n.*856G>A
ENST00000489173.1:n.1787G>A
NM_145262.3:c.1493G>A	NP_660305.2:p.Gly498Asp
NR_026699.1:n.1591G>A
NR_026700.1:n.697G>A
NR_026701.1:n.1589G>A
NR_026702.1:n.627G>A
XM_005264878.2:c.*612G>A	XP_005264935.1:n.*612G>A
XR_245095.2:n.2744G>A
XM_017005730.1:c.1112G>A	XP_016861219.1:p.Gly371Asp
XM_024453351.1:c.1493G>A	XP_024309119.1:p.Gly498Asp
XM_024453352.1:c.*612G>A	XP_024309120.1:n.*612G>A
XR_001740022.2:n.3395G>A
XR_001740023.2:n.2919G>A
XR_245095.4:n.2745G>A
NM_145262.4:c.1493G>A MANE Select	NP_660305.2:p.Gly498Asp
NR_026699.2:n.1583G>A
NR_026700.2:n.689G>A
NR_026701.2:n.1581G>A
NR_026702.2:n.619G>A
NM_001144951.2:c.*612G>A	NP_001138423.1:n.*612G>A