Canonical Allele Identifier: CA1364789186

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292959C= , CM000665.2:g.52292959C=	GRCh38
NC_000003.11:g.52326975C= , CM000665.1:g.52326975C=	GRCh37
NC_000003.10:g.52302015C=	NCBI36
NG_023246.1:g.10140C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1405C= MANE Select	ENSP00000389175.2:p.Leu469=
ENST00000305690.12:c.*524C=	ENSP00000301965.9:n.*524C=
ENST00000436784.6:c.1405C=	ENSP00000389175.2:p.Leu469=
ENST00000461183.5:c.764-87C=	ENSP00000417264.1:n.764-87C=
ENST00000471180.5:c.635-87C=	ENSP00000417526.1:n.635-87C=
ENST00000473032.5:c.530-87C=	ENSP00000418951.1:n.530-87C=
ENST00000477382.1:c.*524C=	ENSP00000419008.1:n.*524C=
ENST00000486393.5:c.*768C=	ENSP00000419868.1:n.*768C=
ENST00000489173.1:n.1699C=
NM_001144951.1:c.*524C=	NP_001138423.1:n.*524C=
NM_145262.3:c.1405C=	NP_660305.2:p.Leu469=
NR_026699.1:n.1503C=
NR_026700.1:n.696-87C=
NR_026701.1:n.1501C=
NR_026702.1:n.626-87C=
XM_005264878.2:c.*524C=	XP_005264935.1:n.*524C=
XR_245095.2:n.2743-87C=
XM_017005730.1:c.1024C=	XP_016861219.1:p.Leu342=
XM_024453351.1:c.1405C=	XP_024309119.1:p.Leu469=
XM_024453352.1:c.*524C=	XP_024309120.1:n.*524C=
XR_001740022.2:n.3307C=
XR_001740023.2:n.2918-87C=
XR_245095.4:n.2744-87C=
NM_145262.4:c.1405C= MANE Select	NP_660305.2:p.Leu469=
NR_026699.2:n.1495C=
NR_026700.2:n.688-87C=
NR_026701.2:n.1493C=
NR_026702.2:n.618-87C=
NM_001144951.2:c.*524C=	NP_001138423.1:n.*524C=