Canonical Allele Identifier: CA1364789316

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293219T= , CM000665.2:g.52293219T=	GRCh38
NC_000003.11:g.52327235T= , CM000665.1:g.52327235T=	GRCh37
NC_000003.10:g.52302275T=	NCBI36
NG_023246.1:g.10400T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*93T= MANE Select	ENSP00000389175.2:n.*93T=
ENST00000436784.6:c.*93T=	ENSP00000389175.2:n.*93T=
ENST00000471180.5:c.*58+27T=	ENSP00000417526.1:n.*58+27T=
ENST00000473032.5:c.*58+27T=	ENSP00000418951.1:n.*58+27T=
ENST00000486393.5:c.*1028T=	ENSP00000419868.1:n.*1028T=
ENST00000489173.1:n.1914+45T=
NM_145262.3:c.*93T=	NP_660305.2:n.*93T=
NR_026699.1:n.1763T=
NR_026700.1:n.842+27T=
NR_026701.1:n.1734+27T=
NR_026702.1:n.772+27T=
XM_005264878.2:c.*784T=	XP_005264935.1:n.*784T=
XR_245095.2:n.2889+27T=
XM_017005730.1:c.*93T=	XP_016861219.1:n.*93T=
XM_024453351.1:c.*93T=	XP_024309119.1:n.*93T=
XM_024453352.1:c.*784T=	XP_024309120.1:n.*784T=
XR_001740022.2:n.3540+27T=
XR_001740023.2:n.3064+27T=
XR_245095.4:n.2890+27T=
NM_145262.4:c.*93T= MANE Select	NP_660305.2:n.*93T=
NR_026699.2:n.1755T=
NR_026700.2:n.834+27T=
NR_026701.2:n.1726+27T=
NR_026702.2:n.764+27T=
NM_001144951.2:c.*784T=	NP_001138423.1:n.*784T=