Canonical Allele Identifier: CA1364789240

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293076A= , CM000665.2:g.52293076A=	GRCh38
NC_000003.11:g.52327092A= , CM000665.1:g.52327092A=	GRCh37
NC_000003.10:g.52302132A=	NCBI36
NG_023246.1:g.10257A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1522A= MANE Select	ENSP00000389175.2:p.Thr508=
ENST00000436784.6:c.1522A=	ENSP00000389175.2:p.Thr508=
ENST00000461183.5:c.794A=	ENSP00000417264.1:p.Asp265=
ENST00000471180.5:c.665A=	ENSP00000417526.1:p.Asp222=
ENST00000473032.5:c.560A=	ENSP00000418951.1:p.Asp187=
ENST00000486393.5:c.*885A=	ENSP00000419868.1:n.*885A=
ENST00000489173.1:n.1816A=
NM_145262.3:c.1522A=	NP_660305.2:p.Thr508=
NR_026699.1:n.1620A=
NR_026700.1:n.726A=
NR_026701.1:n.1618A=
NR_026702.1:n.656A=
XM_005264878.2:c.*641A=	XP_005264935.1:n.*641A=
XR_245095.2:n.2773A=
XM_017005730.1:c.1141A=	XP_016861219.1:p.Thr381=
XM_024453351.1:c.1522A=	XP_024309119.1:p.Thr508=
XM_024453352.1:c.*641A=	XP_024309120.1:n.*641A=
XR_001740022.2:n.3424A=
XR_001740023.2:n.2948A=
XR_245095.4:n.2774A=
NM_145262.4:c.1522A= MANE Select	NP_660305.2:p.Thr508=
NR_026699.2:n.1612A=
NR_026700.2:n.718A=
NR_026701.2:n.1610A=
NR_026702.2:n.648A=
NM_001144951.2:c.*641A=	NP_001138423.1:n.*641A=