Canonical Allele Identifier: CA1364789284

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293165C= , CM000665.2:g.52293165C=	GRCh38
NC_000003.11:g.52327181C= , CM000665.1:g.52327181C=	GRCh37
NC_000003.10:g.52302221C=	NCBI36
NG_023246.1:g.10346C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*39C= MANE Select	ENSP00000389175.2:n.*39C=
ENST00000436784.6:c.*39C=	ENSP00000389175.2:n.*39C=
ENST00000461183.5:c.*31C=	ENSP00000417264.1:n.*31C=
ENST00000471180.5:c.*31C=	ENSP00000417526.1:n.*31C=
ENST00000473032.5:c.*31C=	ENSP00000418951.1:n.*31C=
ENST00000486393.5:c.*974C=	ENSP00000419868.1:n.*974C=
ENST00000489173.1:n.1905C=
NM_145262.3:c.*39C=	NP_660305.2:n.*39C=
NR_026699.1:n.1709C=
NR_026700.1:n.815C=
NR_026701.1:n.1707C=
NR_026702.1:n.745C=
XM_005264878.2:c.*730C=	XP_005264935.1:n.*730C=
XR_245095.2:n.2862C=
XM_017005730.1:c.*39C=	XP_016861219.1:n.*39C=
XM_024453351.1:c.*39C=	XP_024309119.1:n.*39C=
XM_024453352.1:c.*730C=	XP_024309120.1:n.*730C=
XR_001740022.2:n.3513C=
XR_001740023.2:n.3037C=
XR_245095.4:n.2863C=
NM_145262.4:c.*39C= MANE Select	NP_660305.2:n.*39C=
NR_026699.2:n.1701C=
NR_026700.2:n.807C=
NR_026701.2:n.1699C=
NR_026702.2:n.737C=
NM_001144951.2:c.*730C=	NP_001138423.1:n.*730C=