Canonical Allele Identifier: CA1364789324

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293231C= , CM000665.2:g.52293231C=	GRCh38
NC_000003.11:g.52327247C= , CM000665.1:g.52327247C=	GRCh37
NC_000003.10:g.52302287C=	NCBI36
NG_023246.1:g.10412C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*105C= MANE Select	ENSP00000389175.2:n.*105C=
ENST00000436784.6:c.*105C=	ENSP00000389175.2:n.*105C=
ENST00000471180.5:c.*58+39C=	ENSP00000417526.1:n.*58+39C=
ENST00000473032.5:c.*58+39C=	ENSP00000418951.1:n.*58+39C=
ENST00000486393.5:c.*1040C=	ENSP00000419868.1:n.*1040C=
ENST00000489173.1:n.1914+57C=
NM_145262.3:c.*105C=	NP_660305.2:n.*105C=
NR_026699.1:n.1775C=
NR_026700.1:n.842+39C=
NR_026701.1:n.1734+39C=
NR_026702.1:n.772+39C=
XM_005264878.2:c.*796C=	XP_005264935.1:n.*796C=
XR_245095.2:n.2889+39C=
XM_017005730.1:c.*105C=	XP_016861219.1:n.*105C=
XM_024453351.1:c.*105C=	XP_024309119.1:n.*105C=
XM_024453352.1:c.*796C=	XP_024309120.1:n.*796C=
XR_001740022.2:n.3540+39C=
XR_001740023.2:n.3064+39C=
XR_245095.4:n.2890+39C=
NM_145262.4:c.*105C= MANE Select	NP_660305.2:n.*105C=
NR_026699.2:n.1767C=
NR_026700.2:n.834+39C=
NR_026701.2:n.1726+39C=
NR_026702.2:n.764+39C=
NM_001144951.2:c.*796C=	NP_001138423.1:n.*796C=