Canonical Allele Identifier: CA1364789247

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293091A= , CM000665.2:g.52293091A=	GRCh38
NC_000003.11:g.52327107A= , CM000665.1:g.52327107A=	GRCh37
NC_000003.10:g.52302147A=	NCBI36
NG_023246.1:g.10272A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1537A= MANE Select	ENSP00000389175.2:p.Met513=
ENST00000436784.6:c.1537A=	ENSP00000389175.2:p.Met513=
ENST00000461183.5:c.809A=	ENSP00000417264.1:p.His270=
ENST00000471180.5:c.680A=	ENSP00000417526.1:p.His227=
ENST00000473032.5:c.575A=	ENSP00000418951.1:p.His192=
ENST00000486393.5:c.*900A=	ENSP00000419868.1:n.*900A=
ENST00000489173.1:n.1831A=
NM_145262.3:c.1537A=	NP_660305.2:p.Met513=
NR_026699.1:n.1635A=
NR_026700.1:n.741A=
NR_026701.1:n.1633A=
NR_026702.1:n.671A=
XM_005264878.2:c.*656A=	XP_005264935.1:n.*656A=
XR_245095.2:n.2788A=
XM_017005730.1:c.1156A=	XP_016861219.1:p.Met386=
XM_024453351.1:c.1537A=	XP_024309119.1:p.Met513=
XM_024453352.1:c.*656A=	XP_024309120.1:n.*656A=
XR_001740022.2:n.3439A=
XR_001740023.2:n.2963A=
XR_245095.4:n.2789A=
NM_145262.4:c.1537A= MANE Select	NP_660305.2:p.Met513=
NR_026699.2:n.1627A=
NR_026700.2:n.733A=
NR_026701.2:n.1625A=
NR_026702.2:n.663A=
NM_001144951.2:c.*656A=	NP_001138423.1:n.*656A=