Canonical Allele Identifier: CA1364789225

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293036C= , CM000665.2:g.52293036C=	GRCh38
NC_000003.11:g.52327052C= , CM000665.1:g.52327052C=	GRCh37
NC_000003.10:g.52302092C=	NCBI36
NG_023246.1:g.10217C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1482C= MANE Select	ENSP00000389175.2:p.Cys494=
ENST00000436784.6:c.1482C=	ENSP00000389175.2:p.Cys494=
ENST00000461183.5:c.764-10C=	ENSP00000417264.1:n.764-10C=
ENST00000471180.5:c.635-10C=	ENSP00000417526.1:n.635-10C=
ENST00000473032.5:c.530-10C=	ENSP00000418951.1:n.530-10C=
ENST00000486393.5:c.*845C=	ENSP00000419868.1:n.*845C=
ENST00000489173.1:n.1776C=
NM_145262.3:c.1482C=	NP_660305.2:p.Cys494=
NR_026699.1:n.1580C=
NR_026700.1:n.696-10C=
NR_026701.1:n.1578C=
NR_026702.1:n.626-10C=
XM_005264878.2:c.*601C=	XP_005264935.1:n.*601C=
XR_245095.2:n.2743-10C=
XM_017005730.1:c.1101C=	XP_016861219.1:p.Cys367=
XM_024453351.1:c.1482C=	XP_024309119.1:p.Cys494=
XM_024453352.1:c.*601C=	XP_024309120.1:n.*601C=
XR_001740022.2:n.3384C=
XR_001740023.2:n.2918-10C=
XR_245095.4:n.2744-10C=
NM_145262.4:c.1482C= MANE Select	NP_660305.2:p.Cys494=
NR_026699.2:n.1572C=
NR_026700.2:n.688-10C=
NR_026701.2:n.1570C=
NR_026702.2:n.618-10C=
NM_001144951.2:c.*601C=	NP_001138423.1:n.*601C=