Canonical Allele Identifier: CA1364789007

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292584A= , CM000665.2:g.52292584A=	GRCh38
NC_000003.11:g.52326600A= , CM000665.1:g.52326600A=	GRCh37
NC_000003.10:g.52301640A=	NCBI36
NG_023246.1:g.9765A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1030A= MANE Select	ENSP00000389175.2:p.Met344=
ENST00000305690.12:c.*149A=	ENSP00000301965.9:n.*149A=
ENST00000436784.6:c.1030A=	ENSP00000389175.2:p.Met344=
ENST00000461183.5:c.763+15A=	ENSP00000417264.1:n.763+15A=
ENST00000471180.5:c.634+15A=	ENSP00000417526.1:n.634+15A=
ENST00000473032.5:c.530-462A=	ENSP00000418951.1:n.530-462A=
ENST00000477382.1:c.*149A=	ENSP00000419008.1:n.*149A=
ENST00000486393.5:c.*393A=	ENSP00000419868.1:n.*393A=
ENST00000489173.1:n.1324A=
NM_001144951.1:c.*149A=	NP_001138423.1:n.*149A=
NM_145262.3:c.1030A=	NP_660305.2:p.Met344=
NR_026699.1:n.1128A=
NR_026700.1:n.695+15A=
NR_026701.1:n.1126A=
NR_026702.1:n.626-462A=
XM_005264878.2:c.*149A=	XP_005264935.1:n.*149A=
XR_245095.2:n.2742+15A=
XM_017005730.1:c.649A=	XP_016861219.1:p.Met217=
XM_024453351.1:c.1030A=	XP_024309119.1:p.Met344=
XM_024453352.1:c.*149A=	XP_024309120.1:n.*149A=
XR_001740022.2:n.2932A=
XR_001740023.2:n.2917+15A=
XR_245095.4:n.2743+15A=
NM_145262.4:c.1030A= MANE Select	NP_660305.2:p.Met344=
NR_026699.2:n.1120A=
NR_026700.2:n.687+15A=
NR_026701.2:n.1118A=
NR_026702.2:n.618-462A=
NM_001144951.2:c.*149A=	NP_001138423.1:n.*149A=