Canonical Allele Identifier: CA1364789188

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292968C= , CM000665.2:g.52292968C=	GRCh38
NC_000003.11:g.52326984C= , CM000665.1:g.52326984C=	GRCh37
NC_000003.10:g.52302024C=	NCBI36
NG_023246.1:g.10149C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1414C= MANE Select	ENSP00000389175.2:p.Gln472=
ENST00000305690.12:c.*533C=	ENSP00000301965.9:n.*533C=
ENST00000436784.6:c.1414C=	ENSP00000389175.2:p.Gln472=
ENST00000461183.5:c.764-78C=	ENSP00000417264.1:n.764-78C=
ENST00000471180.5:c.635-78C=	ENSP00000417526.1:n.635-78C=
ENST00000473032.5:c.530-78C=	ENSP00000418951.1:n.530-78C=
ENST00000477382.1:c.*533C=	ENSP00000419008.1:n.*533C=
ENST00000486393.5:c.*777C=	ENSP00000419868.1:n.*777C=
ENST00000489173.1:n.1708C=
NM_001144951.1:c.*533C=	NP_001138423.1:n.*533C=
NM_145262.3:c.1414C=	NP_660305.2:p.Gln472=
NR_026699.1:n.1512C=
NR_026700.1:n.696-78C=
NR_026701.1:n.1510C=
NR_026702.1:n.626-78C=
XM_005264878.2:c.*533C=	XP_005264935.1:n.*533C=
XR_245095.2:n.2743-78C=
XM_017005730.1:c.1033C=	XP_016861219.1:p.Gln345=
XM_024453351.1:c.1414C=	XP_024309119.1:p.Gln472=
XM_024453352.1:c.*533C=	XP_024309120.1:n.*533C=
XR_001740022.2:n.3316C=
XR_001740023.2:n.2918-78C=
XR_245095.4:n.2744-78C=
NM_145262.4:c.1414C= MANE Select	NP_660305.2:p.Gln472=
NR_026699.2:n.1504C=
NR_026700.2:n.688-78C=
NR_026701.2:n.1502C=
NR_026702.2:n.618-78C=
NM_001144951.2:c.*533C=	NP_001138423.1:n.*533C=