Canonical Allele Identifier: CA353076552

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293047-G-T
• MyVariant Identifiers: chr3:g.52327063G>T (hg19) ; chr3:g.52293047G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1493G>T MANE Select	ENSP00000389175.2:p.Gly498Val
ENST00000436784.6:c.1493G>T	ENSP00000389175.2:p.Gly498Val
ENST00000461183.5:c.765G>T	ENSP00000417264.1:p.Gly255=
ENST00000471180.5:c.636G>T	ENSP00000417526.1:p.Gly212=
ENST00000473032.5:c.531G>T	ENSP00000418951.1:p.Gly177=
ENST00000486393.5:c.*856G>T	ENSP00000419868.1:n.*856G>T
ENST00000489173.1:n.1787G>T
NM_145262.3:c.1493G>T	NP_660305.2:p.Gly498Val
NR_026699.1:n.1591G>T
NR_026700.1:n.697G>T
NR_026701.1:n.1589G>T
NR_026702.1:n.627G>T
XM_005264878.2:c.*612G>T	XP_005264935.1:n.*612G>T
XR_245095.2:n.2744G>T
XM_017005730.1:c.1112G>T	XP_016861219.1:p.Gly371Val
XM_024453351.1:c.1493G>T	XP_024309119.1:p.Gly498Val
XM_024453352.1:c.*612G>T	XP_024309120.1:n.*612G>T
XR_001740022.2:n.3395G>T
XR_001740023.2:n.2919G>T
XR_245095.4:n.2745G>T
NM_145262.4:c.1493G>T MANE Select	NP_660305.2:p.Gly498Val
NR_026699.2:n.1583G>T
NR_026700.2:n.689G>T
NR_026701.2:n.1581G>T
NR_026702.2:n.619G>T
NM_001144951.2:c.*612G>T	NP_001138423.1:n.*612G>T