Canonical Allele Identifier: CA353076649

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327087G>A (hg19) ; chr3:g.52293071G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293071G>A , CM000665.2:g.52293071G>A	GRCh38
NC_000003.11:g.52327087G>A , CM000665.1:g.52327087G>A	GRCh37
NC_000003.10:g.52302127G>A	NCBI36
NG_023246.1:g.10252G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1517G>A MANE Select	ENSP00000389175.2:p.Gly506Glu
ENST00000436784.6:c.1517G>A	ENSP00000389175.2:p.Gly506Glu
ENST00000461183.5:c.789G>A	ENSP00000417264.1:p.Arg263=
ENST00000471180.5:c.660G>A	ENSP00000417526.1:p.Arg220=
ENST00000473032.5:c.555G>A	ENSP00000418951.1:p.Arg185=
ENST00000486393.5:c.*880G>A	ENSP00000419868.1:n.*880G>A
ENST00000489173.1:n.1811G>A
NM_145262.3:c.1517G>A	NP_660305.2:p.Gly506Glu
NR_026699.1:n.1615G>A
NR_026700.1:n.721G>A
NR_026701.1:n.1613G>A
NR_026702.1:n.651G>A
XM_005264878.2:c.*636G>A	XP_005264935.1:n.*636G>A
XR_245095.2:n.2768G>A
XM_017005730.1:c.1136G>A	XP_016861219.1:p.Gly379Glu
XM_024453351.1:c.1517G>A	XP_024309119.1:p.Gly506Glu
XM_024453352.1:c.*636G>A	XP_024309120.1:n.*636G>A
XR_001740022.2:n.3419G>A
XR_001740023.2:n.2943G>A
XR_245095.4:n.2769G>A
NM_145262.4:c.1517G>A MANE Select	NP_660305.2:p.Gly506Glu
NR_026699.2:n.1607G>A
NR_026700.2:n.713G>A
NR_026701.2:n.1605G>A
NR_026702.2:n.643G>A
NM_001144951.2:c.*636G>A	NP_001138423.1:n.*636G>A