Canonical Allele Identifier: CA1364789335

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293254G= , CM000665.2:g.52293254G=	GRCh38
NC_000003.11:g.52327270G= , CM000665.1:g.52327270G=	GRCh37
NC_000003.10:g.52302310G=	NCBI36
NG_023246.1:g.10435G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*128G= MANE Select	ENSP00000389175.2:n.*128G=
ENST00000436784.6:c.*128G=	ENSP00000389175.2:n.*128G=
ENST00000471180.5:c.*59-53G=	ENSP00000417526.1:n.*59-53G=
ENST00000473032.5:c.*59-53G=	ENSP00000418951.1:n.*59-53G=
ENST00000486393.5:c.*1063G=	ENSP00000419868.1:n.*1063G=
ENST00000489173.1:n.1915-53G=
NM_145262.3:c.*128G=	NP_660305.2:n.*128G=
NR_026699.1:n.1798G=
NR_026700.1:n.843-53G=
NR_026701.1:n.1735-53G=
NR_026702.1:n.773-53G=
XM_005264878.2:c.*819G=	XP_005264935.1:n.*819G=
XR_245095.2:n.2890-53G=
XM_017005730.1:c.*128G=	XP_016861219.1:n.*128G=
XM_024453351.1:c.*128G=	XP_024309119.1:n.*128G=
XM_024453352.1:c.*819G=	XP_024309120.1:n.*819G=
XR_001740022.2:n.3541-53G=
XR_001740023.2:n.3065-53G=
XR_245095.4:n.2891-53G=
NM_145262.4:c.*128G= MANE Select	NP_660305.2:n.*128G=
NR_026699.2:n.1790G=
NR_026700.2:n.835-53G=
NR_026701.2:n.1727-53G=
NR_026702.2:n.765-53G=
NM_001144951.2:c.*819G=	NP_001138423.1:n.*819G=