Canonical Allele Identifier: CA1364789261

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293119C= , CM000665.2:g.52293119C=	GRCh38
NC_000003.11:g.52327135C= , CM000665.1:g.52327135C=	GRCh37
NC_000003.10:g.52302175C=	NCBI36
NG_023246.1:g.10300C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1565C= MANE Select	ENSP00000389175.2:p.Pro522=
ENST00000436784.6:c.1565C=	ENSP00000389175.2:p.Pro522=
ENST00000461183.5:c.837C=	ENSP00000417264.1:p.Ala279=
ENST00000471180.5:c.708C=	ENSP00000417526.1:p.Ala236=
ENST00000473032.5:c.603C=	ENSP00000418951.1:p.Ala201=
ENST00000486393.5:c.*928C=	ENSP00000419868.1:n.*928C=
ENST00000489173.1:n.1859C=
NM_145262.3:c.1565C=	NP_660305.2:p.Pro522=
NR_026699.1:n.1663C=
NR_026700.1:n.769C=
NR_026701.1:n.1661C=
NR_026702.1:n.699C=
XM_005264878.2:c.*684C=	XP_005264935.1:n.*684C=
XR_245095.2:n.2816C=
XM_017005730.1:c.1184C=	XP_016861219.1:p.Pro395=
XM_024453351.1:c.1565C=	XP_024309119.1:p.Pro522=
XM_024453352.1:c.*684C=	XP_024309120.1:n.*684C=
XR_001740022.2:n.3467C=
XR_001740023.2:n.2991C=
XR_245095.4:n.2817C=
NM_145262.4:c.1565C= MANE Select	NP_660305.2:p.Pro522=
NR_026699.2:n.1655C=
NR_026700.2:n.761C=
NR_026701.2:n.1653C=
NR_026702.2:n.691C=
NM_001144951.2:c.*684C=	NP_001138423.1:n.*684C=