Canonical Allele Identifier: CA1364789337

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293259C= , CM000665.2:g.52293259C=	GRCh38
NC_000003.11:g.52327275C= , CM000665.1:g.52327275C=	GRCh37
NC_000003.10:g.52302315C=	NCBI36
NG_023246.1:g.10440C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*133C= MANE Select	ENSP00000389175.2:n.*133C=
ENST00000436784.6:c.*133C=	ENSP00000389175.2:n.*133C=
ENST00000471180.5:c.*59-48C=	ENSP00000417526.1:n.*59-48C=
ENST00000473032.5:c.*59-48C=	ENSP00000418951.1:n.*59-48C=
ENST00000486393.5:c.*1068C=	ENSP00000419868.1:n.*1068C=
ENST00000489173.1:n.1915-48C=
NM_145262.3:c.*133C=	NP_660305.2:n.*133C=
NR_026699.1:n.1803C=
NR_026700.1:n.843-48C=
NR_026701.1:n.1735-48C=
NR_026702.1:n.773-48C=
XM_005264878.2:c.*824C=	XP_005264935.1:n.*824C=
XR_245095.2:n.2890-48C=
XM_017005730.1:c.*133C=	XP_016861219.1:n.*133C=
XM_024453351.1:c.*133C=	XP_024309119.1:n.*133C=
XM_024453352.1:c.*824C=	XP_024309120.1:n.*824C=
XR_001740022.2:n.3541-48C=
XR_001740023.2:n.3065-48C=
XR_245095.4:n.2891-48C=
NM_145262.4:c.*133C= MANE Select	NP_660305.2:n.*133C=
NR_026699.2:n.1795C=
NR_026700.2:n.835-48C=
NR_026701.2:n.1727-48C=
NR_026702.2:n.765-48C=
NM_001144951.2:c.*824C=	NP_001138423.1:n.*824C=