Canonical Allele Identifier: CA1364789219

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293025A= , CM000665.2:g.52293025A=	GRCh38
NC_000003.11:g.52327041A= , CM000665.1:g.52327041A=	GRCh37
NC_000003.10:g.52302081A=	NCBI36
NG_023246.1:g.10206A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1471A= MANE Select	ENSP00000389175.2:p.Thr491=
ENST00000436784.6:c.1471A=	ENSP00000389175.2:p.Thr491=
ENST00000461183.5:c.764-21A=	ENSP00000417264.1:n.764-21A=
ENST00000471180.5:c.635-21A=	ENSP00000417526.1:n.635-21A=
ENST00000473032.5:c.530-21A=	ENSP00000418951.1:n.530-21A=
ENST00000486393.5:c.*834A=	ENSP00000419868.1:n.*834A=
ENST00000489173.1:n.1765A=
NM_145262.3:c.1471A=	NP_660305.2:p.Thr491=
NR_026699.1:n.1569A=
NR_026700.1:n.696-21A=
NR_026701.1:n.1567A=
NR_026702.1:n.626-21A=
XM_005264878.2:c.*590A=	XP_005264935.1:n.*590A=
XR_245095.2:n.2743-21A=
XM_017005730.1:c.1090A=	XP_016861219.1:p.Thr364=
XM_024453351.1:c.1471A=	XP_024309119.1:p.Thr491=
XM_024453352.1:c.*590A=	XP_024309120.1:n.*590A=
XR_001740022.2:n.3373A=
XR_001740023.2:n.2918-21A=
XR_245095.4:n.2744-21A=
NM_145262.4:c.1471A= MANE Select	NP_660305.2:p.Thr491=
NR_026699.2:n.1561A=
NR_026700.2:n.688-21A=
NR_026701.2:n.1559A=
NR_026702.2:n.618-21A=
NM_001144951.2:c.*590A=	NP_001138423.1:n.*590A=