Canonical Allele Identifier: CA1364789314

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293217C= , CM000665.2:g.52293217C=	GRCh38
NC_000003.11:g.52327233C= , CM000665.1:g.52327233C=	GRCh37
NC_000003.10:g.52302273C=	NCBI36
NG_023246.1:g.10398C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*91C= MANE Select	ENSP00000389175.2:n.*91C=
ENST00000436784.6:c.*91C=	ENSP00000389175.2:n.*91C=
ENST00000471180.5:c.*58+25C=	ENSP00000417526.1:n.*58+25C=
ENST00000473032.5:c.*58+25C=	ENSP00000418951.1:n.*58+25C=
ENST00000486393.5:c.*1026C=	ENSP00000419868.1:n.*1026C=
ENST00000489173.1:n.1914+43C=
NM_145262.3:c.*91C=	NP_660305.2:n.*91C=
NR_026699.1:n.1761C=
NR_026700.1:n.842+25C=
NR_026701.1:n.1734+25C=
NR_026702.1:n.772+25C=
XM_005264878.2:c.*782C=	XP_005264935.1:n.*782C=
XR_245095.2:n.2889+25C=
XM_017005730.1:c.*91C=	XP_016861219.1:n.*91C=
XM_024453351.1:c.*91C=	XP_024309119.1:n.*91C=
XM_024453352.1:c.*782C=	XP_024309120.1:n.*782C=
XR_001740022.2:n.3540+25C=
XR_001740023.2:n.3064+25C=
XR_245095.4:n.2890+25C=
NM_145262.4:c.*91C= MANE Select	NP_660305.2:n.*91C=
NR_026699.2:n.1753C=
NR_026700.2:n.834+25C=
NR_026701.2:n.1726+25C=
NR_026702.2:n.764+25C=
NM_001144951.2:c.*782C=	NP_001138423.1:n.*782C=