Canonical Allele Identifier: CA1364789259

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293115C= , CM000665.2:g.52293115C=	GRCh38
NC_000003.11:g.52327131C= , CM000665.1:g.52327131C=	GRCh37
NC_000003.10:g.52302171C=	NCBI36
NG_023246.1:g.10296C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1561C= MANE Select	ENSP00000389175.2:p.Arg521=
ENST00000436784.6:c.1561C=	ENSP00000389175.2:p.Arg521=
ENST00000461183.5:c.833C=	ENSP00000417264.1:p.Ala278=
ENST00000471180.5:c.704C=	ENSP00000417526.1:p.Ala235=
ENST00000473032.5:c.599C=	ENSP00000418951.1:p.Ala200=
ENST00000486393.5:c.*924C=	ENSP00000419868.1:n.*924C=
ENST00000489173.1:n.1855C=
NM_145262.3:c.1561C=	NP_660305.2:p.Arg521=
NR_026699.1:n.1659C=
NR_026700.1:n.765C=
NR_026701.1:n.1657C=
NR_026702.1:n.695C=
XM_005264878.2:c.*680C=	XP_005264935.1:n.*680C=
XR_245095.2:n.2812C=
XM_017005730.1:c.1180C=	XP_016861219.1:p.Arg394=
XM_024453351.1:c.1561C=	XP_024309119.1:p.Arg521=
XM_024453352.1:c.*680C=	XP_024309120.1:n.*680C=
XR_001740022.2:n.3463C=
XR_001740023.2:n.2987C=
XR_245095.4:n.2813C=
NM_145262.4:c.1561C= MANE Select	NP_660305.2:p.Arg521=
NR_026699.2:n.1651C=
NR_026700.2:n.757C=
NR_026701.2:n.1649C=
NR_026702.2:n.687C=
NM_001144951.2:c.*680C=	NP_001138423.1:n.*680C=