Canonical Allele Identifier: CA1364789238

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293070G= , CM000665.2:g.52293070G=	GRCh38
NC_000003.11:g.52327086G= , CM000665.1:g.52327086G=	GRCh37
NC_000003.10:g.52302126G=	NCBI36
NG_023246.1:g.10251G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1516G= MANE Select	ENSP00000389175.2:p.Gly506=
ENST00000436784.6:c.1516G=	ENSP00000389175.2:p.Gly506=
ENST00000461183.5:c.788G=	ENSP00000417264.1:p.Arg263=
ENST00000471180.5:c.659G=	ENSP00000417526.1:p.Arg220=
ENST00000473032.5:c.554G=	ENSP00000418951.1:p.Arg185=
ENST00000486393.5:c.*879G=	ENSP00000419868.1:n.*879G=
ENST00000489173.1:n.1810G=
NM_145262.3:c.1516G=	NP_660305.2:p.Gly506=
NR_026699.1:n.1614G=
NR_026700.1:n.720G=
NR_026701.1:n.1612G=
NR_026702.1:n.650G=
XM_005264878.2:c.*635G=	XP_005264935.1:n.*635G=
XR_245095.2:n.2767G=
XM_017005730.1:c.1135G=	XP_016861219.1:p.Gly379=
XM_024453351.1:c.1516G=	XP_024309119.1:p.Gly506=
XM_024453352.1:c.*635G=	XP_024309120.1:n.*635G=
XR_001740022.2:n.3418G=
XR_001740023.2:n.2942G=
XR_245095.4:n.2768G=
NM_145262.4:c.1516G= MANE Select	NP_660305.2:p.Gly506=
NR_026699.2:n.1606G=
NR_026700.2:n.712G=
NR_026701.2:n.1604G=
NR_026702.2:n.642G=
NM_001144951.2:c.*635G=	NP_001138423.1:n.*635G=