Canonical Allele Identifier: CA2756266617

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293100del , CM000665.2:g.52293100del	GRCh38
NC_000003.11:g.52327116del , CM000665.1:g.52327116del	GRCh37
NC_000003.10:g.52302156del	NCBI36
NG_023246.1:g.10281del

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1546del MANE Select	ENSP00000389175.2:p.His516ThrfsTer?
ENST00000436784.6:c.1546del	ENSP00000389175.2:p.His516ThrfsTer?
ENST00000461183.5:c.818del	ENSP00000417264.1:p.Pro273HisfsTer9
ENST00000471180.5:c.689del	ENSP00000417526.1:p.Pro230HisfsTer9
ENST00000473032.5:c.584del	ENSP00000418951.1:p.Pro195HisfsTer9
ENST00000486393.5:c.*909del	ENSP00000419868.1:n.*909del
ENST00000489173.1:n.1840del
NM_145262.3:c.1546del	NP_660305.2:p.His516ThrfsTer?
NR_026699.1:n.1644del
NR_026700.1:n.750del
NR_026701.1:n.1642del
NR_026702.1:n.680del
XM_005264878.2:c.*665del	XP_005264935.1:n.*665del
XR_245095.2:n.2797del
XM_017005730.1:c.1165del	XP_016861219.1:p.His389ThrfsTer?
XM_024453351.1:c.1546del	XP_024309119.1:p.His516ThrfsTer?
XM_024453352.1:c.*665del	XP_024309120.1:n.*665del
XR_001740022.2:n.3448del
XR_001740023.2:n.2972del
XR_245095.4:n.2798del
NM_145262.4:c.1546del MANE Select	NP_660305.2:p.His516ThrfsTer?
NR_026699.2:n.1636del
NR_026700.2:n.742del
NR_026701.2:n.1634del
NR_026702.2:n.672del
NM_001144951.2:c.*665del	NP_001138423.1:n.*665del