Canonical Allele Identifier: CA1364789208

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293010C= , CM000665.2:g.52293010C=	GRCh38
NC_000003.11:g.52327026C= , CM000665.1:g.52327026C=	GRCh37
NC_000003.10:g.52302066C=	NCBI36
NG_023246.1:g.10191C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1456C= MANE Select	ENSP00000389175.2:p.His486=
ENST00000436784.6:c.1456C=	ENSP00000389175.2:p.His486=
ENST00000461183.5:c.764-36C=	ENSP00000417264.1:n.764-36C=
ENST00000471180.5:c.635-36C=	ENSP00000417526.1:n.635-36C=
ENST00000473032.5:c.530-36C=	ENSP00000418951.1:n.530-36C=
ENST00000486393.5:c.*819C=	ENSP00000419868.1:n.*819C=
ENST00000489173.1:n.1750C=
NM_145262.3:c.1456C=	NP_660305.2:p.His486=
NR_026699.1:n.1554C=
NR_026700.1:n.696-36C=
NR_026701.1:n.1552C=
NR_026702.1:n.626-36C=
XM_005264878.2:c.*575C=	XP_005264935.1:n.*575C=
XR_245095.2:n.2743-36C=
XM_017005730.1:c.1075C=	XP_016861219.1:p.His359=
XM_024453351.1:c.1456C=	XP_024309119.1:p.His486=
XM_024453352.1:c.*575C=	XP_024309120.1:n.*575C=
XR_001740022.2:n.3358C=
XR_001740023.2:n.2918-36C=
XR_245095.4:n.2744-36C=
NM_145262.4:c.1456C= MANE Select	NP_660305.2:p.His486=
NR_026699.2:n.1546C=
NR_026700.2:n.688-36C=
NR_026701.2:n.1544C=
NR_026702.2:n.618-36C=
NM_001144951.2:c.*575C=	NP_001138423.1:n.*575C=