Canonical Allele Identifier: CA1364789228

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293045G= , CM000665.2:g.52293045G=	GRCh38
NC_000003.11:g.52327061G= , CM000665.1:g.52327061G=	GRCh37
NC_000003.10:g.52302101G=	NCBI36
NG_023246.1:g.10226G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1491G= MANE Select	ENSP00000389175.2:p.Gln497=
ENST00000436784.6:c.1491G=	ENSP00000389175.2:p.Gln497=
ENST00000461183.5:c.764-1G=	ENSP00000417264.1:n.764-1G=
ENST00000471180.5:c.635-1G=	ENSP00000417526.1:n.635-1G=
ENST00000473032.5:c.530-1G=	ENSP00000418951.1:n.530-1G=
ENST00000486393.5:c.*854G=	ENSP00000419868.1:n.*854G=
ENST00000489173.1:n.1785G=
NM_145262.3:c.1491G=	NP_660305.2:p.Gln497=
NR_026699.1:n.1589G=
NR_026700.1:n.696-1G=
NR_026701.1:n.1587G=
NR_026702.1:n.626-1G=
XM_005264878.2:c.*610G=	XP_005264935.1:n.*610G=
XR_245095.2:n.2743-1G=
XM_017005730.1:c.1110G=	XP_016861219.1:p.Gln370=
XM_024453351.1:c.1491G=	XP_024309119.1:p.Gln497=
XM_024453352.1:c.*610G=	XP_024309120.1:n.*610G=
XR_001740022.2:n.3393G=
XR_001740023.2:n.2918-1G=
XR_245095.4:n.2744-1G=
NM_145262.4:c.1491G= MANE Select	NP_660305.2:p.Gln497=
NR_026699.2:n.1581G=
NR_026700.2:n.688-1G=
NR_026701.2:n.1579G=
NR_026702.2:n.618-1G=
NM_001144951.2:c.*610G=	NP_001138423.1:n.*610G=