Canonical Allele Identifier: CA1364789307

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293204G= , CM000665.2:g.52293204G=	GRCh38
NC_000003.11:g.52327220G= , CM000665.1:g.52327220G=	GRCh37
NC_000003.10:g.52302260G=	NCBI36
NG_023246.1:g.10385G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*78G= MANE Select	ENSP00000389175.2:n.*78G=
ENST00000436784.6:c.*78G=	ENSP00000389175.2:n.*78G=
ENST00000471180.5:c.*58+12G=	ENSP00000417526.1:n.*58+12G=
ENST00000473032.5:c.*58+12G=	ENSP00000418951.1:n.*58+12G=
ENST00000486393.5:c.*1013G=	ENSP00000419868.1:n.*1013G=
ENST00000489173.1:n.1914+30G=
NM_145262.3:c.*78G=	NP_660305.2:n.*78G=
NR_026699.1:n.1748G=
NR_026700.1:n.842+12G=
NR_026701.1:n.1734+12G=
NR_026702.1:n.772+12G=
XM_005264878.2:c.*769G=	XP_005264935.1:n.*769G=
XR_245095.2:n.2889+12G=
XM_017005730.1:c.*78G=	XP_016861219.1:n.*78G=
XM_024453351.1:c.*78G=	XP_024309119.1:n.*78G=
XM_024453352.1:c.*769G=	XP_024309120.1:n.*769G=
XR_001740022.2:n.3540+12G=
XR_001740023.2:n.3064+12G=
XR_245095.4:n.2890+12G=
NM_145262.4:c.*78G= MANE Select	NP_660305.2:n.*78G=
NR_026699.2:n.1740G=
NR_026700.2:n.834+12G=
NR_026701.2:n.1726+12G=
NR_026702.2:n.764+12G=
NM_001144951.2:c.*769G=	NP_001138423.1:n.*769G=