Canonical Allele Identifier: CA1364789271

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293140A= , CM000665.2:g.52293140A=	GRCh38
NC_000003.11:g.52327156A= , CM000665.1:g.52327156A=	GRCh37
NC_000003.10:g.52302196A=	NCBI36
NG_023246.1:g.10321A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.*14A= MANE Select	ENSP00000389175.2:n.*14A=
ENST00000436784.6:c.*14A=	ENSP00000389175.2:n.*14A=
ENST00000461183.5:c.*6A=	ENSP00000417264.1:n.*6A=
ENST00000471180.5:c.*6A=	ENSP00000417526.1:n.*6A=
ENST00000473032.5:c.*6A=	ENSP00000418951.1:n.*6A=
ENST00000486393.5:c.*949A=	ENSP00000419868.1:n.*949A=
ENST00000489173.1:n.1880A=
NM_145262.3:c.*14A=	NP_660305.2:n.*14A=
NR_026699.1:n.1684A=
NR_026700.1:n.790A=
NR_026701.1:n.1682A=
NR_026702.1:n.720A=
XM_005264878.2:c.*705A=	XP_005264935.1:n.*705A=
XR_245095.2:n.2837A=
XM_017005730.1:c.*14A=	XP_016861219.1:n.*14A=
XM_024453351.1:c.*14A=	XP_024309119.1:n.*14A=
XM_024453352.1:c.*705A=	XP_024309120.1:n.*705A=
XR_001740022.2:n.3488A=
XR_001740023.2:n.3012A=
XR_245095.4:n.2838A=
NM_145262.4:c.*14A= MANE Select	NP_660305.2:n.*14A=
NR_026699.2:n.1676A=
NR_026700.2:n.782A=
NR_026701.2:n.1674A=
NR_026702.2:n.712A=
NM_001144951.2:c.*705A=	NP_001138423.1:n.*705A=