Canonical Allele Identifier: CA1364789243

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293083C= , CM000665.2:g.52293083C=	GRCh38
NC_000003.11:g.52327099C= , CM000665.1:g.52327099C=	GRCh37
NC_000003.10:g.52302139C=	NCBI36
NG_023246.1:g.10264C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1529C= MANE Select	ENSP00000389175.2:p.Thr510=
ENST00000436784.6:c.1529C=	ENSP00000389175.2:p.Thr510=
ENST00000461183.5:c.801C=	ENSP00000417264.1:p.Tyr267=
ENST00000471180.5:c.672C=	ENSP00000417526.1:p.Tyr224=
ENST00000473032.5:c.567C=	ENSP00000418951.1:p.Tyr189=
ENST00000486393.5:c.*892C=	ENSP00000419868.1:n.*892C=
ENST00000489173.1:n.1823C=
NM_145262.3:c.1529C=	NP_660305.2:p.Thr510=
NR_026699.1:n.1627C=
NR_026700.1:n.733C=
NR_026701.1:n.1625C=
NR_026702.1:n.663C=
XM_005264878.2:c.*648C=	XP_005264935.1:n.*648C=
XR_245095.2:n.2780C=
XM_017005730.1:c.1148C=	XP_016861219.1:p.Thr383=
XM_024453351.1:c.1529C=	XP_024309119.1:p.Thr510=
XM_024453352.1:c.*648C=	XP_024309120.1:n.*648C=
XR_001740022.2:n.3431C=
XR_001740023.2:n.2955C=
XR_245095.4:n.2781C=
NM_145262.4:c.1529C= MANE Select	NP_660305.2:p.Thr510=
NR_026699.2:n.1619C=
NR_026700.2:n.725C=
NR_026701.2:n.1617C=
NR_026702.2:n.655C=
NM_001144951.2:c.*648C=	NP_001138423.1:n.*648C=