Canonical Allele Identifier: CA1364789268

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293130C= , CM000665.2:g.52293130C=	GRCh38
NC_000003.11:g.52327146C= , CM000665.1:g.52327146C=	GRCh37
NC_000003.10:g.52302186C=	NCBI36
NG_023246.1:g.10311C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.*4C= MANE Select	ENSP00000389175.2:n.*4C=
ENST00000436784.6:c.*4C=	ENSP00000389175.2:n.*4C=
ENST00000461183.5:c.848C=	ENSP00000417264.1:p.Ala283=
ENST00000471180.5:c.719C=	ENSP00000417526.1:p.Ala240=
ENST00000473032.5:c.614C=	ENSP00000418951.1:p.Ala205=
ENST00000486393.5:c.*939C=	ENSP00000419868.1:n.*939C=
ENST00000489173.1:n.1870C=
NM_145262.3:c.*4C=	NP_660305.2:n.*4C=
NR_026699.1:n.1674C=
NR_026700.1:n.780C=
NR_026701.1:n.1672C=
NR_026702.1:n.710C=
XM_005264878.2:c.*695C=	XP_005264935.1:n.*695C=
XR_245095.2:n.2827C=
XM_017005730.1:c.*4C=	XP_016861219.1:n.*4C=
XM_024453351.1:c.*4C=	XP_024309119.1:n.*4C=
XM_024453352.1:c.*695C=	XP_024309120.1:n.*695C=
XR_001740022.2:n.3478C=
XR_001740023.2:n.3002C=
XR_245095.4:n.2828C=
NM_145262.4:c.*4C= MANE Select	NP_660305.2:n.*4C=
NR_026699.2:n.1666C=
NR_026700.2:n.772C=
NR_026701.2:n.1664C=
NR_026702.2:n.702C=
NM_001144951.2:c.*695C=	NP_001138423.1:n.*695C=