Canonical Allele Identifier: CA1364789304

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293200C= , CM000665.2:g.52293200C=	GRCh38
NC_000003.11:g.52327216C= , CM000665.1:g.52327216C=	GRCh37
NC_000003.10:g.52302256C=	NCBI36
NG_023246.1:g.10381C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*74C= MANE Select	ENSP00000389175.2:n.*74C=
ENST00000436784.6:c.*74C=	ENSP00000389175.2:n.*74C=
ENST00000471180.5:c.*58+8C=	ENSP00000417526.1:n.*58+8C=
ENST00000473032.5:c.*58+8C=	ENSP00000418951.1:n.*58+8C=
ENST00000486393.5:c.*1009C=	ENSP00000419868.1:n.*1009C=
ENST00000489173.1:n.1914+26C=
NM_145262.3:c.*74C=	NP_660305.2:n.*74C=
NR_026699.1:n.1744C=
NR_026700.1:n.842+8C=
NR_026701.1:n.1734+8C=
NR_026702.1:n.772+8C=
XM_005264878.2:c.*765C=	XP_005264935.1:n.*765C=
XR_245095.2:n.2889+8C=
XM_017005730.1:c.*74C=	XP_016861219.1:n.*74C=
XM_024453351.1:c.*74C=	XP_024309119.1:n.*74C=
XM_024453352.1:c.*765C=	XP_024309120.1:n.*765C=
XR_001740022.2:n.3540+8C=
XR_001740023.2:n.3064+8C=
XR_245095.4:n.2890+8C=
NM_145262.4:c.*74C= MANE Select	NP_660305.2:n.*74C=
NR_026699.2:n.1736C=
NR_026700.2:n.834+8C=
NR_026701.2:n.1726+8C=
NR_026702.2:n.764+8C=
NM_001144951.2:c.*765C=	NP_001138423.1:n.*765C=