Canonical Allele Identifier: CA1364789137

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292855T= , CM000665.2:g.52292855T=	GRCh38
NC_000003.11:g.52326871T= , CM000665.1:g.52326871T=	GRCh37
NC_000003.10:g.52301911T=	NCBI36
NG_023246.1:g.10036T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1301T= MANE Select	ENSP00000389175.2:p.Leu434=
ENST00000305690.12:c.*420T=	ENSP00000301965.9:n.*420T=
ENST00000436784.6:c.1301T=	ENSP00000389175.2:p.Leu434=
ENST00000461183.5:c.764-191T=	ENSP00000417264.1:n.764-191T=
ENST00000471180.5:c.635-191T=	ENSP00000417526.1:n.635-191T=
ENST00000473032.5:c.530-191T=	ENSP00000418951.1:n.530-191T=
ENST00000477382.1:c.*420T=	ENSP00000419008.1:n.*420T=
ENST00000486393.5:c.*664T=	ENSP00000419868.1:n.*664T=
ENST00000489173.1:n.1595T=
NM_001144951.1:c.*420T=	NP_001138423.1:n.*420T=
NM_145262.3:c.1301T=	NP_660305.2:p.Leu434=
NR_026699.1:n.1399T=
NR_026700.1:n.696-191T=
NR_026701.1:n.1397T=
NR_026702.1:n.626-191T=
XM_005264878.2:c.*420T=	XP_005264935.1:n.*420T=
XR_245095.2:n.2743-191T=
XM_017005730.1:c.920T=	XP_016861219.1:p.Leu307=
XM_024453351.1:c.1301T=	XP_024309119.1:p.Leu434=
XM_024453352.1:c.*420T=	XP_024309120.1:n.*420T=
XR_001740022.2:n.3203T=
XR_001740023.2:n.2918-191T=
XR_245095.4:n.2744-191T=
NM_145262.4:c.1301T= MANE Select	NP_660305.2:p.Leu434=
NR_026699.2:n.1391T=
NR_026700.2:n.688-191T=
NR_026701.2:n.1389T=
NR_026702.2:n.618-191T=
NM_001144951.2:c.*420T=	NP_001138423.1:n.*420T=