Canonical Allele Identifier: CA1364789253

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293100C= , CM000665.2:g.52293100C=	GRCh38
NC_000003.11:g.52327116C= , CM000665.1:g.52327116C=	GRCh37
NC_000003.10:g.52302156C=	NCBI36
NG_023246.1:g.10281C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1546C= MANE Select	ENSP00000389175.2:p.His516=
ENST00000436784.6:c.1546C=	ENSP00000389175.2:p.His516=
ENST00000461183.5:c.818C=	ENSP00000417264.1:p.Pro273=
ENST00000471180.5:c.689C=	ENSP00000417526.1:p.Pro230=
ENST00000473032.5:c.584C=	ENSP00000418951.1:p.Pro195=
ENST00000486393.5:c.*909C=	ENSP00000419868.1:n.*909C=
ENST00000489173.1:n.1840C=
NM_145262.3:c.1546C=	NP_660305.2:p.His516=
NR_026699.1:n.1644C=
NR_026700.1:n.750C=
NR_026701.1:n.1642C=
NR_026702.1:n.680C=
XM_005264878.2:c.*665C=	XP_005264935.1:n.*665C=
XR_245095.2:n.2797C=
XM_017005730.1:c.1165C=	XP_016861219.1:p.His389=
XM_024453351.1:c.1546C=	XP_024309119.1:p.His516=
XM_024453352.1:c.*665C=	XP_024309120.1:n.*665C=
XR_001740022.2:n.3448C=
XR_001740023.2:n.2972C=
XR_245095.4:n.2798C=
NM_145262.4:c.1546C= MANE Select	NP_660305.2:p.His516=
NR_026699.2:n.1636C=
NR_026700.2:n.742C=
NR_026701.2:n.1634C=
NR_026702.2:n.672C=
NM_001144951.2:c.*665C=	NP_001138423.1:n.*665C=