Canonical Allele Identifier: CA1364789232

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293054A= , CM000665.2:g.52293054A=	GRCh38
NC_000003.11:g.52327070A= , CM000665.1:g.52327070A=	GRCh37
NC_000003.10:g.52302110A=	NCBI36
NG_023246.1:g.10235A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1500A= MANE Select	ENSP00000389175.2:p.Ala500=
ENST00000436784.6:c.1500A=	ENSP00000389175.2:p.Ala500=
ENST00000461183.5:c.772A=	ENSP00000417264.1:p.Thr258=
ENST00000471180.5:c.643A=	ENSP00000417526.1:p.Thr215=
ENST00000473032.5:c.538A=	ENSP00000418951.1:p.Thr180=
ENST00000486393.5:c.*863A=	ENSP00000419868.1:n.*863A=
ENST00000489173.1:n.1794A=
NM_145262.3:c.1500A=	NP_660305.2:p.Ala500=
NR_026699.1:n.1598A=
NR_026700.1:n.704A=
NR_026701.1:n.1596A=
NR_026702.1:n.634A=
XM_005264878.2:c.*619A=	XP_005264935.1:n.*619A=
XR_245095.2:n.2751A=
XM_017005730.1:c.1119A=	XP_016861219.1:p.Ala373=
XM_024453351.1:c.1500A=	XP_024309119.1:p.Ala500=
XM_024453352.1:c.*619A=	XP_024309120.1:n.*619A=
XR_001740022.2:n.3402A=
XR_001740023.2:n.2926A=
XR_245095.4:n.2752A=
NM_145262.4:c.1500A= MANE Select	NP_660305.2:p.Ala500=
NR_026699.2:n.1590A=
NR_026700.2:n.696A=
NR_026701.2:n.1588A=
NR_026702.2:n.626A=
NM_001144951.2:c.*619A=	NP_001138423.1:n.*619A=