Canonical Allele Identifier: CA1364789196

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292984G= , CM000665.2:g.52292984G=	GRCh38
NC_000003.11:g.52327000G= , CM000665.1:g.52327000G=	GRCh37
NC_000003.10:g.52302040G=	NCBI36
NG_023246.1:g.10165G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1430G= MANE Select	ENSP00000389175.2:p.Gly477=
ENST00000305690.12:c.*549G=	ENSP00000301965.9:n.*549G=
ENST00000436784.6:c.1430G=	ENSP00000389175.2:p.Gly477=
ENST00000461183.5:c.764-62G=	ENSP00000417264.1:n.764-62G=
ENST00000471180.5:c.635-62G=	ENSP00000417526.1:n.635-62G=
ENST00000473032.5:c.530-62G=	ENSP00000418951.1:n.530-62G=
ENST00000477382.1:c.*549G=	ENSP00000419008.1:n.*549G=
ENST00000486393.5:c.*793G=	ENSP00000419868.1:n.*793G=
ENST00000489173.1:n.1724G=
NM_001144951.1:c.*549G=	NP_001138423.1:n.*549G=
NM_145262.3:c.1430G=	NP_660305.2:p.Gly477=
NR_026699.1:n.1528G=
NR_026700.1:n.696-62G=
NR_026701.1:n.1526G=
NR_026702.1:n.626-62G=
XM_005264878.2:c.*549G=	XP_005264935.1:n.*549G=
XR_245095.2:n.2743-62G=
XM_017005730.1:c.1049G=	XP_016861219.1:p.Gly350=
XM_024453351.1:c.1430G=	XP_024309119.1:p.Gly477=
XM_024453352.1:c.*549G=	XP_024309120.1:n.*549G=
XR_001740022.2:n.3332G=
XR_001740023.2:n.2918-62G=
XR_245095.4:n.2744-62G=
NM_145262.4:c.1430G= MANE Select	NP_660305.2:p.Gly477=
NR_026699.2:n.1520G=
NR_026700.2:n.688-62G=
NR_026701.2:n.1518G=
NR_026702.2:n.618-62G=
NM_001144951.2:c.*549G=	NP_001138423.1:n.*549G=