Canonical Allele Identifier: CA1364789308

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293206G= , CM000665.2:g.52293206G=	GRCh38
NC_000003.11:g.52327222G= , CM000665.1:g.52327222G=	GRCh37
NC_000003.10:g.52302262G=	NCBI36
NG_023246.1:g.10387G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*80G= MANE Select	ENSP00000389175.2:n.*80G=
ENST00000436784.6:c.*80G=	ENSP00000389175.2:n.*80G=
ENST00000471180.5:c.*58+14G=	ENSP00000417526.1:n.*58+14G=
ENST00000473032.5:c.*58+14G=	ENSP00000418951.1:n.*58+14G=
ENST00000486393.5:c.*1015G=	ENSP00000419868.1:n.*1015G=
ENST00000489173.1:n.1914+32G=
NM_145262.3:c.*80G=	NP_660305.2:n.*80G=
NR_026699.1:n.1750G=
NR_026700.1:n.842+14G=
NR_026701.1:n.1734+14G=
NR_026702.1:n.772+14G=
XM_005264878.2:c.*771G=	XP_005264935.1:n.*771G=
XR_245095.2:n.2889+14G=
XM_017005730.1:c.*80G=	XP_016861219.1:n.*80G=
XM_024453351.1:c.*80G=	XP_024309119.1:n.*80G=
XM_024453352.1:c.*771G=	XP_024309120.1:n.*771G=
XR_001740022.2:n.3540+14G=
XR_001740023.2:n.3064+14G=
XR_245095.4:n.2890+14G=
NM_145262.4:c.*80G= MANE Select	NP_660305.2:n.*80G=
NR_026699.2:n.1742G=
NR_026700.2:n.834+14G=
NR_026701.2:n.1726+14G=
NR_026702.2:n.764+14G=
NM_001144951.2:c.*771G=	NP_001138423.1:n.*771G=