Canonical Allele Identifier: CA1364789235

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293063G= , CM000665.2:g.52293063G=	GRCh38
NC_000003.11:g.52327079G= , CM000665.1:g.52327079G=	GRCh37
NC_000003.10:g.52302119G=	NCBI36
NG_023246.1:g.10244G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1509G= MANE Select	ENSP00000389175.2:p.Leu503=
ENST00000436784.6:c.1509G=	ENSP00000389175.2:p.Leu503=
ENST00000461183.5:c.781G=	ENSP00000417264.1:p.Ala261=
ENST00000471180.5:c.652G=	ENSP00000417526.1:p.Ala218=
ENST00000473032.5:c.547G=	ENSP00000418951.1:p.Ala183=
ENST00000486393.5:c.*872G=	ENSP00000419868.1:n.*872G=
ENST00000489173.1:n.1803G=
NM_145262.3:c.1509G=	NP_660305.2:p.Leu503=
NR_026699.1:n.1607G=
NR_026700.1:n.713G=
NR_026701.1:n.1605G=
NR_026702.1:n.643G=
XM_005264878.2:c.*628G=	XP_005264935.1:n.*628G=
XR_245095.2:n.2760G=
XM_017005730.1:c.1128G=	XP_016861219.1:p.Leu376=
XM_024453351.1:c.1509G=	XP_024309119.1:p.Leu503=
XM_024453352.1:c.*628G=	XP_024309120.1:n.*628G=
XR_001740022.2:n.3411G=
XR_001740023.2:n.2935G=
XR_245095.4:n.2761G=
NM_145262.4:c.1509G= MANE Select	NP_660305.2:p.Leu503=
NR_026699.2:n.1599G=
NR_026700.2:n.705G=
NR_026701.2:n.1597G=
NR_026702.2:n.635G=
NM_001144951.2:c.*628G=	NP_001138423.1:n.*628G=