Canonical Allele Identifier: CA1364789218

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293023A= , CM000665.2:g.52293023A=	GRCh38
NC_000003.11:g.52327039A= , CM000665.1:g.52327039A=	GRCh37
NC_000003.10:g.52302079A=	NCBI36
NG_023246.1:g.10204A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1469A= MANE Select	ENSP00000389175.2:p.His490=
ENST00000436784.6:c.1469A=	ENSP00000389175.2:p.His490=
ENST00000461183.5:c.764-23A=	ENSP00000417264.1:n.764-23A=
ENST00000471180.5:c.635-23A=	ENSP00000417526.1:n.635-23A=
ENST00000473032.5:c.530-23A=	ENSP00000418951.1:n.530-23A=
ENST00000486393.5:c.*832A=	ENSP00000419868.1:n.*832A=
ENST00000489173.1:n.1763A=
NM_145262.3:c.1469A=	NP_660305.2:p.His490=
NR_026699.1:n.1567A=
NR_026700.1:n.696-23A=
NR_026701.1:n.1565A=
NR_026702.1:n.626-23A=
XM_005264878.2:c.*588A=	XP_005264935.1:n.*588A=
XR_245095.2:n.2743-23A=
XM_017005730.1:c.1088A=	XP_016861219.1:p.His363=
XM_024453351.1:c.1469A=	XP_024309119.1:p.His490=
XM_024453352.1:c.*588A=	XP_024309120.1:n.*588A=
XR_001740022.2:n.3371A=
XR_001740023.2:n.2918-23A=
XR_245095.4:n.2744-23A=
NM_145262.4:c.1469A= MANE Select	NP_660305.2:p.His490=
NR_026699.2:n.1559A=
NR_026700.2:n.688-23A=
NR_026701.2:n.1557A=
NR_026702.2:n.618-23A=
NM_001144951.2:c.*588A=	NP_001138423.1:n.*588A=