Canonical Allele Identifier: CA1364789251

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293098C= , CM000665.2:g.52293098C=	GRCh38
NC_000003.11:g.52327114C= , CM000665.1:g.52327114C=	GRCh37
NC_000003.10:g.52302154C=	NCBI36
NG_023246.1:g.10279C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1544C= MANE Select	ENSP00000389175.2:p.Thr515=
ENST00000436784.6:c.1544C=	ENSP00000389175.2:p.Thr515=
ENST00000461183.5:c.816C=	ENSP00000417264.1:p.His272=
ENST00000471180.5:c.687C=	ENSP00000417526.1:p.His229=
ENST00000473032.5:c.582C=	ENSP00000418951.1:p.His194=
ENST00000486393.5:c.*907C=	ENSP00000419868.1:n.*907C=
ENST00000489173.1:n.1838C=
NM_145262.3:c.1544C=	NP_660305.2:p.Thr515=
NR_026699.1:n.1642C=
NR_026700.1:n.748C=
NR_026701.1:n.1640C=
NR_026702.1:n.678C=
XM_005264878.2:c.*663C=	XP_005264935.1:n.*663C=
XR_245095.2:n.2795C=
XM_017005730.1:c.1163C=	XP_016861219.1:p.Thr388=
XM_024453351.1:c.1544C=	XP_024309119.1:p.Thr515=
XM_024453352.1:c.*663C=	XP_024309120.1:n.*663C=
XR_001740022.2:n.3446C=
XR_001740023.2:n.2970C=
XR_245095.4:n.2796C=
NM_145262.4:c.1544C= MANE Select	NP_660305.2:p.Thr515=
NR_026699.2:n.1634C=
NR_026700.2:n.740C=
NR_026701.2:n.1632C=
NR_026702.2:n.670C=
NM_001144951.2:c.*663C=	NP_001138423.1:n.*663C=