Canonical Allele Identifier: CA1364789350

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293284G= , CM000665.2:g.52293284G=	GRCh38
NC_000003.11:g.52327300G= , CM000665.1:g.52327300G=	GRCh37
NC_000003.10:g.52302340G=	NCBI36
NG_023246.1:g.10465G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*158G= MANE Select	ENSP00000389175.2:n.*158G=
ENST00000436784.6:c.*158G=	ENSP00000389175.2:n.*158G=
ENST00000471180.5:c.*59-23G=	ENSP00000417526.1:n.*59-23G=
ENST00000473032.5:c.*59-23G=	ENSP00000418951.1:n.*59-23G=
ENST00000486393.5:c.*1093G=	ENSP00000419868.1:n.*1093G=
ENST00000489173.1:n.1915-23G=
NM_145262.3:c.*158G=	NP_660305.2:n.*158G=
NR_026699.1:n.1828G=
NR_026700.1:n.843-23G=
NR_026701.1:n.1735-23G=
NR_026702.1:n.773-23G=
XM_005264878.2:c.*849G=	XP_005264935.1:n.*849G=
XR_245095.2:n.2890-23G=
XM_017005730.1:c.*158G=	XP_016861219.1:n.*158G=
XM_024453351.1:c.*158G=	XP_024309119.1:n.*158G=
XM_024453352.1:c.*849G=	XP_024309120.1:n.*849G=
XR_001740022.2:n.3541-23G=
XR_001740023.2:n.3065-23G=
XR_245095.4:n.2891-23G=
NM_145262.4:c.*158G= MANE Select	NP_660305.2:n.*158G=
NR_026699.2:n.1820G=
NR_026700.2:n.835-23G=
NR_026701.2:n.1727-23G=
NR_026702.2:n.765-23G=
NM_001144951.2:c.*849G=	NP_001138423.1:n.*849G=