Canonical Allele Identifier: CA1364789331

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293241C= , CM000665.2:g.52293241C=	GRCh38
NC_000003.11:g.52327257C= , CM000665.1:g.52327257C=	GRCh37
NC_000003.10:g.52302297C=	NCBI36
NG_023246.1:g.10422C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*115C= MANE Select	ENSP00000389175.2:n.*115C=
ENST00000436784.6:c.*115C=	ENSP00000389175.2:n.*115C=
ENST00000471180.5:c.*58+49C=	ENSP00000417526.1:n.*58+49C=
ENST00000473032.5:c.*58+49C=	ENSP00000418951.1:n.*58+49C=
ENST00000486393.5:c.*1050C=	ENSP00000419868.1:n.*1050C=
ENST00000489173.1:n.1915-66C=
NM_145262.3:c.*115C=	NP_660305.2:n.*115C=
NR_026699.1:n.1785C=
NR_026700.1:n.842+49C=
NR_026701.1:n.1734+49C=
NR_026702.1:n.772+49C=
XM_005264878.2:c.*806C=	XP_005264935.1:n.*806C=
XR_245095.2:n.2889+49C=
XM_017005730.1:c.*115C=	XP_016861219.1:n.*115C=
XM_024453351.1:c.*115C=	XP_024309119.1:n.*115C=
XM_024453352.1:c.*806C=	XP_024309120.1:n.*806C=
XR_001740022.2:n.3540+49C=
XR_001740023.2:n.3064+49C=
XR_245095.4:n.2890+49C=
NM_145262.4:c.*115C= MANE Select	NP_660305.2:n.*115C=
NR_026699.2:n.1777C=
NR_026700.2:n.834+49C=
NR_026701.2:n.1726+49C=
NR_026702.2:n.764+49C=
NM_001144951.2:c.*806C=	NP_001138423.1:n.*806C=