Canonical Allele Identifier: CA1364789202

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293002T= , CM000665.2:g.52293002T=	GRCh38
NC_000003.11:g.52327018T= , CM000665.1:g.52327018T=	GRCh37
NC_000003.10:g.52302058T=	NCBI36
NG_023246.1:g.10183T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1448T= MANE Select	ENSP00000389175.2:p.Phe483=
ENST00000305690.12:c.*567T=	ENSP00000301965.9:n.*567T=
ENST00000436784.6:c.1448T=	ENSP00000389175.2:p.Phe483=
ENST00000461183.5:c.764-44T=	ENSP00000417264.1:n.764-44T=
ENST00000471180.5:c.635-44T=	ENSP00000417526.1:n.635-44T=
ENST00000473032.5:c.530-44T=	ENSP00000418951.1:n.530-44T=
ENST00000477382.1:c.*567T=	ENSP00000419008.1:n.*567T=
ENST00000486393.5:c.*811T=	ENSP00000419868.1:n.*811T=
ENST00000489173.1:n.1742T=
NM_001144951.1:c.*567T=	NP_001138423.1:n.*567T=
NM_145262.3:c.1448T=	NP_660305.2:p.Phe483=
NR_026699.1:n.1546T=
NR_026700.1:n.696-44T=
NR_026701.1:n.1544T=
NR_026702.1:n.626-44T=
XM_005264878.2:c.*567T=	XP_005264935.1:n.*567T=
XR_245095.2:n.2743-44T=
XM_017005730.1:c.1067T=	XP_016861219.1:p.Phe356=
XM_024453351.1:c.1448T=	XP_024309119.1:p.Phe483=
XM_024453352.1:c.*567T=	XP_024309120.1:n.*567T=
XR_001740022.2:n.3350T=
XR_001740023.2:n.2918-44T=
XR_245095.4:n.2744-44T=
NM_145262.4:c.1448T= MANE Select	NP_660305.2:p.Phe483=
NR_026699.2:n.1538T=
NR_026700.2:n.688-44T=
NR_026701.2:n.1536T=
NR_026702.2:n.618-44T=
NM_001144951.2:c.*567T=	NP_001138423.1:n.*567T=