Canonical Allele Identifier: CA1364789223

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293032T= , CM000665.2:g.52293032T=	GRCh38
NC_000003.11:g.52327048T= , CM000665.1:g.52327048T=	GRCh37
NC_000003.10:g.52302088T=	NCBI36
NG_023246.1:g.10213T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1478T= MANE Select	ENSP00000389175.2:p.Phe493=
ENST00000436784.6:c.1478T=	ENSP00000389175.2:p.Phe493=
ENST00000461183.5:c.764-14T=	ENSP00000417264.1:n.764-14T=
ENST00000471180.5:c.635-14T=	ENSP00000417526.1:n.635-14T=
ENST00000473032.5:c.530-14T=	ENSP00000418951.1:n.530-14T=
ENST00000486393.5:c.*841T=	ENSP00000419868.1:n.*841T=
ENST00000489173.1:n.1772T=
NM_145262.3:c.1478T=	NP_660305.2:p.Phe493=
NR_026699.1:n.1576T=
NR_026700.1:n.696-14T=
NR_026701.1:n.1574T=
NR_026702.1:n.626-14T=
XM_005264878.2:c.*597T=	XP_005264935.1:n.*597T=
XR_245095.2:n.2743-14T=
XM_017005730.1:c.1097T=	XP_016861219.1:p.Phe366=
XM_024453351.1:c.1478T=	XP_024309119.1:p.Phe493=
XM_024453352.1:c.*597T=	XP_024309120.1:n.*597T=
XR_001740022.2:n.3380T=
XR_001740023.2:n.2918-14T=
XR_245095.4:n.2744-14T=
NM_145262.4:c.1478T= MANE Select	NP_660305.2:p.Phe493=
NR_026699.2:n.1568T=
NR_026700.2:n.688-14T=
NR_026701.2:n.1566T=
NR_026702.2:n.618-14T=
NM_001144951.2:c.*597T=	NP_001138423.1:n.*597T=