Canonical Allele Identifier: CA1364789182

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292951C= , CM000665.2:g.52292951C=	GRCh38
NC_000003.11:g.52326967C= , CM000665.1:g.52326967C=	GRCh37
NC_000003.10:g.52302007C=	NCBI36
NG_023246.1:g.10132C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1397C= MANE Select	ENSP00000389175.2:p.Thr466=
ENST00000305690.12:c.*516C=	ENSP00000301965.9:n.*516C=
ENST00000436784.6:c.1397C=	ENSP00000389175.2:p.Thr466=
ENST00000461183.5:c.764-95C=	ENSP00000417264.1:n.764-95C=
ENST00000471180.5:c.635-95C=	ENSP00000417526.1:n.635-95C=
ENST00000473032.5:c.530-95C=	ENSP00000418951.1:n.530-95C=
ENST00000477382.1:c.*516C=	ENSP00000419008.1:n.*516C=
ENST00000486393.5:c.*760C=	ENSP00000419868.1:n.*760C=
ENST00000489173.1:n.1691C=
NM_001144951.1:c.*516C=	NP_001138423.1:n.*516C=
NM_145262.3:c.1397C=	NP_660305.2:p.Thr466=
NR_026699.1:n.1495C=
NR_026700.1:n.696-95C=
NR_026701.1:n.1493C=
NR_026702.1:n.626-95C=
XM_005264878.2:c.*516C=	XP_005264935.1:n.*516C=
XR_245095.2:n.2743-95C=
XM_017005730.1:c.1016C=	XP_016861219.1:p.Thr339=
XM_024453351.1:c.1397C=	XP_024309119.1:p.Thr466=
XM_024453352.1:c.*516C=	XP_024309120.1:n.*516C=
XR_001740022.2:n.3299C=
XR_001740023.2:n.2918-95C=
XR_245095.4:n.2744-95C=
NM_145262.4:c.1397C= MANE Select	NP_660305.2:p.Thr466=
NR_026699.2:n.1487C=
NR_026700.2:n.688-95C=
NR_026701.2:n.1485C=
NR_026702.2:n.618-95C=
NM_001144951.2:c.*516C=	NP_001138423.1:n.*516C=