Canonical Allele Identifier: CA1364789328

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293238T= , CM000665.2:g.52293238T=	GRCh38
NC_000003.11:g.52327254T= , CM000665.1:g.52327254T=	GRCh37
NC_000003.10:g.52302294T=	NCBI36
NG_023246.1:g.10419T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*112T= MANE Select	ENSP00000389175.2:n.*112T=
ENST00000436784.6:c.*112T=	ENSP00000389175.2:n.*112T=
ENST00000471180.5:c.*58+46T=	ENSP00000417526.1:n.*58+46T=
ENST00000473032.5:c.*58+46T=	ENSP00000418951.1:n.*58+46T=
ENST00000486393.5:c.*1047T=	ENSP00000419868.1:n.*1047T=
ENST00000489173.1:n.1914+64T=
NM_145262.3:c.*112T=	NP_660305.2:n.*112T=
NR_026699.1:n.1782T=
NR_026700.1:n.842+46T=
NR_026701.1:n.1734+46T=
NR_026702.1:n.772+46T=
XM_005264878.2:c.*803T=	XP_005264935.1:n.*803T=
XR_245095.2:n.2889+46T=
XM_017005730.1:c.*112T=	XP_016861219.1:n.*112T=
XM_024453351.1:c.*112T=	XP_024309119.1:n.*112T=
XM_024453352.1:c.*803T=	XP_024309120.1:n.*803T=
XR_001740022.2:n.3540+46T=
XR_001740023.2:n.3064+46T=
XR_245095.4:n.2890+46T=
NM_145262.4:c.*112T= MANE Select	NP_660305.2:n.*112T=
NR_026699.2:n.1774T=
NR_026700.2:n.834+46T=
NR_026701.2:n.1726+46T=
NR_026702.2:n.764+46T=
NM_001144951.2:c.*803T=	NP_001138423.1:n.*803T=