Canonical Allele Identifier: CA1364789200

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292992A= , CM000665.2:g.52292992A=	GRCh38
NC_000003.11:g.52327008A= , CM000665.1:g.52327008A=	GRCh37
NC_000003.10:g.52302048A=	NCBI36
NG_023246.1:g.10173A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1438A= MANE Select	ENSP00000389175.2:p.Ile480=
ENST00000305690.12:c.*557A=	ENSP00000301965.9:n.*557A=
ENST00000436784.6:c.1438A=	ENSP00000389175.2:p.Ile480=
ENST00000461183.5:c.764-54A=	ENSP00000417264.1:n.764-54A=
ENST00000471180.5:c.635-54A=	ENSP00000417526.1:n.635-54A=
ENST00000473032.5:c.530-54A=	ENSP00000418951.1:n.530-54A=
ENST00000477382.1:c.*557A=	ENSP00000419008.1:n.*557A=
ENST00000486393.5:c.*801A=	ENSP00000419868.1:n.*801A=
ENST00000489173.1:n.1732A=
NM_001144951.1:c.*557A=	NP_001138423.1:n.*557A=
NM_145262.3:c.1438A=	NP_660305.2:p.Ile480=
NR_026699.1:n.1536A=
NR_026700.1:n.696-54A=
NR_026701.1:n.1534A=
NR_026702.1:n.626-54A=
XM_005264878.2:c.*557A=	XP_005264935.1:n.*557A=
XR_245095.2:n.2743-54A=
XM_017005730.1:c.1057A=	XP_016861219.1:p.Ile353=
XM_024453351.1:c.1438A=	XP_024309119.1:p.Ile480=
XM_024453352.1:c.*557A=	XP_024309120.1:n.*557A=
XR_001740022.2:n.3340A=
XR_001740023.2:n.2918-54A=
XR_245095.4:n.2744-54A=
NM_145262.4:c.1438A= MANE Select	NP_660305.2:p.Ile480=
NR_026699.2:n.1528A=
NR_026700.2:n.688-54A=
NR_026701.2:n.1526A=
NR_026702.2:n.618-54A=
NM_001144951.2:c.*557A=	NP_001138423.1:n.*557A=