Canonical Allele Identifier: CA1364789078

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292732A= , CM000665.2:g.52292732A=	GRCh38
NC_000003.11:g.52326748A= , CM000665.1:g.52326748A=	GRCh37
NC_000003.10:g.52301788A=	NCBI36
NG_023246.1:g.9913A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1178A= MANE Select	ENSP00000389175.2:p.Glu393=
ENST00000305690.12:c.*297A=	ENSP00000301965.9:n.*297A=
ENST00000436784.6:c.1178A=	ENSP00000389175.2:p.Glu393=
ENST00000461183.5:c.763+163A=	ENSP00000417264.1:n.763+163A=
ENST00000471180.5:c.634+163A=	ENSP00000417526.1:n.634+163A=
ENST00000473032.5:c.530-314A=	ENSP00000418951.1:n.530-314A=
ENST00000477382.1:c.*297A=	ENSP00000419008.1:n.*297A=
ENST00000486393.5:c.*541A=	ENSP00000419868.1:n.*541A=
ENST00000489173.1:n.1472A=
NM_001144951.1:c.*297A=	NP_001138423.1:n.*297A=
NM_145262.3:c.1178A=	NP_660305.2:p.Glu393=
NR_026699.1:n.1276A=
NR_026700.1:n.695+163A=
NR_026701.1:n.1274A=
NR_026702.1:n.626-314A=
XM_005264878.2:c.*297A=	XP_005264935.1:n.*297A=
XR_245095.2:n.2742+163A=
XM_017005730.1:c.797A=	XP_016861219.1:p.Glu266=
XM_024453351.1:c.1178A=	XP_024309119.1:p.Glu393=
XM_024453352.1:c.*297A=	XP_024309120.1:n.*297A=
XR_001740022.2:n.3080A=
XR_001740023.2:n.2917+163A=
XR_245095.4:n.2743+163A=
NM_145262.4:c.1178A= MANE Select	NP_660305.2:p.Glu393=
NR_026699.2:n.1268A=
NR_026700.2:n.687+163A=
NR_026701.2:n.1266A=
NR_026702.2:n.618-314A=
NM_001144951.2:c.*297A=	NP_001138423.1:n.*297A=