Canonical Allele Identifier: CA1364789273

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293146G= , CM000665.2:g.52293146G=	GRCh38
NC_000003.11:g.52327162G= , CM000665.1:g.52327162G=	GRCh37
NC_000003.10:g.52302202G=	NCBI36
NG_023246.1:g.10327G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*20G= MANE Select	ENSP00000389175.2:n.*20G=
ENST00000436784.6:c.*20G=	ENSP00000389175.2:n.*20G=
ENST00000461183.5:c.*12G=	ENSP00000417264.1:n.*12G=
ENST00000471180.5:c.*12G=	ENSP00000417526.1:n.*12G=
ENST00000473032.5:c.*12G=	ENSP00000418951.1:n.*12G=
ENST00000486393.5:c.*955G=	ENSP00000419868.1:n.*955G=
ENST00000489173.1:n.1886G=
NM_145262.3:c.*20G=	NP_660305.2:n.*20G=
NR_026699.1:n.1690G=
NR_026700.1:n.796G=
NR_026701.1:n.1688G=
NR_026702.1:n.726G=
XM_005264878.2:c.*711G=	XP_005264935.1:n.*711G=
XR_245095.2:n.2843G=
XM_017005730.1:c.*20G=	XP_016861219.1:n.*20G=
XM_024453351.1:c.*20G=	XP_024309119.1:n.*20G=
XM_024453352.1:c.*711G=	XP_024309120.1:n.*711G=
XR_001740022.2:n.3494G=
XR_001740023.2:n.3018G=
XR_245095.4:n.2844G=
NM_145262.4:c.*20G= MANE Select	NP_660305.2:n.*20G=
NR_026699.2:n.1682G=
NR_026700.2:n.788G=
NR_026701.2:n.1680G=
NR_026702.2:n.718G=
NM_001144951.2:c.*711G=	NP_001138423.1:n.*711G=