Canonical Allele Identifier: CA1364789167

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292911G= , CM000665.2:g.52292911G=	GRCh38
NC_000003.11:g.52326927G= , CM000665.1:g.52326927G=	GRCh37
NC_000003.10:g.52301967G=	NCBI36
NG_023246.1:g.10092G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1357G= MANE Select	ENSP00000389175.2:p.Gly453=
ENST00000305690.12:c.*476G=	ENSP00000301965.9:n.*476G=
ENST00000436784.6:c.1357G=	ENSP00000389175.2:p.Gly453=
ENST00000461183.5:c.764-135G=	ENSP00000417264.1:n.764-135G=
ENST00000471180.5:c.635-135G=	ENSP00000417526.1:n.635-135G=
ENST00000473032.5:c.530-135G=	ENSP00000418951.1:n.530-135G=
ENST00000477382.1:c.*476G=	ENSP00000419008.1:n.*476G=
ENST00000486393.5:c.*720G=	ENSP00000419868.1:n.*720G=
ENST00000489173.1:n.1651G=
NM_001144951.1:c.*476G=	NP_001138423.1:n.*476G=
NM_145262.3:c.1357G=	NP_660305.2:p.Gly453=
NR_026699.1:n.1455G=
NR_026700.1:n.696-135G=
NR_026701.1:n.1453G=
NR_026702.1:n.626-135G=
XM_005264878.2:c.*476G=	XP_005264935.1:n.*476G=
XR_245095.2:n.2743-135G=
XM_017005730.1:c.976G=	XP_016861219.1:p.Gly326=
XM_024453351.1:c.1357G=	XP_024309119.1:p.Gly453=
XM_024453352.1:c.*476G=	XP_024309120.1:n.*476G=
XR_001740022.2:n.3259G=
XR_001740023.2:n.2918-135G=
XR_245095.4:n.2744-135G=
NM_145262.4:c.1357G= MANE Select	NP_660305.2:p.Gly453=
NR_026699.2:n.1447G=
NR_026700.2:n.688-135G=
NR_026701.2:n.1445G=
NR_026702.2:n.618-135G=
NM_001144951.2:c.*476G=	NP_001138423.1:n.*476G=