Canonical Allele Identifier: CA1364789233

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293055C= , CM000665.2:g.52293055C=	GRCh38
NC_000003.11:g.52327071C= , CM000665.1:g.52327071C=	GRCh37
NC_000003.10:g.52302111C=	NCBI36
NG_023246.1:g.10236C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1501C= MANE Select	ENSP00000389175.2:p.His501=
ENST00000436784.6:c.1501C=	ENSP00000389175.2:p.His501=
ENST00000461183.5:c.773C=	ENSP00000417264.1:p.Thr258=
ENST00000471180.5:c.644C=	ENSP00000417526.1:p.Thr215=
ENST00000473032.5:c.539C=	ENSP00000418951.1:p.Thr180=
ENST00000486393.5:c.*864C=	ENSP00000419868.1:n.*864C=
ENST00000489173.1:n.1795C=
NM_145262.3:c.1501C=	NP_660305.2:p.His501=
NR_026699.1:n.1599C=
NR_026700.1:n.705C=
NR_026701.1:n.1597C=
NR_026702.1:n.635C=
XM_005264878.2:c.*620C=	XP_005264935.1:n.*620C=
XR_245095.2:n.2752C=
XM_017005730.1:c.1120C=	XP_016861219.1:p.His374=
XM_024453351.1:c.1501C=	XP_024309119.1:p.His501=
XM_024453352.1:c.*620C=	XP_024309120.1:n.*620C=
XR_001740022.2:n.3403C=
XR_001740023.2:n.2927C=
XR_245095.4:n.2753C=
NM_145262.4:c.1501C= MANE Select	NP_660305.2:p.His501=
NR_026699.2:n.1591C=
NR_026700.2:n.697C=
NR_026701.2:n.1589C=
NR_026702.2:n.627C=
NM_001144951.2:c.*620C=	NP_001138423.1:n.*620C=