Canonical Allele Identifier: CA1364789193

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292979T= , CM000665.2:g.52292979T=	GRCh38
NC_000003.11:g.52326995T= , CM000665.1:g.52326995T=	GRCh37
NC_000003.10:g.52302035T=	NCBI36
NG_023246.1:g.10160T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1425T= MANE Select	ENSP00000389175.2:p.Ala475=
ENST00000305690.12:c.*544T=	ENSP00000301965.9:n.*544T=
ENST00000436784.6:c.1425T=	ENSP00000389175.2:p.Ala475=
ENST00000461183.5:c.764-67T=	ENSP00000417264.1:n.764-67T=
ENST00000471180.5:c.635-67T=	ENSP00000417526.1:n.635-67T=
ENST00000473032.5:c.530-67T=	ENSP00000418951.1:n.530-67T=
ENST00000477382.1:c.*544T=	ENSP00000419008.1:n.*544T=
ENST00000486393.5:c.*788T=	ENSP00000419868.1:n.*788T=
ENST00000489173.1:n.1719T=
NM_001144951.1:c.*544T=	NP_001138423.1:n.*544T=
NM_145262.3:c.1425T=	NP_660305.2:p.Ala475=
NR_026699.1:n.1523T=
NR_026700.1:n.696-67T=
NR_026701.1:n.1521T=
NR_026702.1:n.626-67T=
XM_005264878.2:c.*544T=	XP_005264935.1:n.*544T=
XR_245095.2:n.2743-67T=
XM_017005730.1:c.1044T=	XP_016861219.1:p.Ala348=
XM_024453351.1:c.1425T=	XP_024309119.1:p.Ala475=
XM_024453352.1:c.*544T=	XP_024309120.1:n.*544T=
XR_001740022.2:n.3327T=
XR_001740023.2:n.2918-67T=
XR_245095.4:n.2744-67T=
NM_145262.4:c.1425T= MANE Select	NP_660305.2:p.Ala475=
NR_026699.2:n.1515T=
NR_026700.2:n.688-67T=
NR_026701.2:n.1513T=
NR_026702.2:n.618-67T=
NM_001144951.2:c.*544T=	NP_001138423.1:n.*544T=