Canonical Allele Identifier: CA1364789234

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293058C= , CM000665.2:g.52293058C=	GRCh38
NC_000003.11:g.52327074C= , CM000665.1:g.52327074C=	GRCh37
NC_000003.10:g.52302114C=	NCBI36
NG_023246.1:g.10239C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1504C= MANE Select	ENSP00000389175.2:p.Leu502=
ENST00000436784.6:c.1504C=	ENSP00000389175.2:p.Leu502=
ENST00000461183.5:c.776C=	ENSP00000417264.1:p.Pro259=
ENST00000471180.5:c.647C=	ENSP00000417526.1:p.Pro216=
ENST00000473032.5:c.542C=	ENSP00000418951.1:p.Pro181=
ENST00000486393.5:c.*867C=	ENSP00000419868.1:n.*867C=
ENST00000489173.1:n.1798C=
NM_145262.3:c.1504C=	NP_660305.2:p.Leu502=
NR_026699.1:n.1602C=
NR_026700.1:n.708C=
NR_026701.1:n.1600C=
NR_026702.1:n.638C=
XM_005264878.2:c.*623C=	XP_005264935.1:n.*623C=
XR_245095.2:n.2755C=
XM_017005730.1:c.1123C=	XP_016861219.1:p.Leu375=
XM_024453351.1:c.1504C=	XP_024309119.1:p.Leu502=
XM_024453352.1:c.*623C=	XP_024309120.1:n.*623C=
XR_001740022.2:n.3406C=
XR_001740023.2:n.2930C=
XR_245095.4:n.2756C=
NM_145262.4:c.1504C= MANE Select	NP_660305.2:p.Leu502=
NR_026699.2:n.1594C=
NR_026700.2:n.700C=
NR_026701.2:n.1592C=
NR_026702.2:n.630C=
NM_001144951.2:c.*623C=	NP_001138423.1:n.*623C=