Canonical Allele Identifier: CA1364789231

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293053C= , CM000665.2:g.52293053C=	GRCh38
NC_000003.11:g.52327069C= , CM000665.1:g.52327069C=	GRCh37
NC_000003.10:g.52302109C=	NCBI36
NG_023246.1:g.10234C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1499C= MANE Select	ENSP00000389175.2:p.Ala500=
ENST00000436784.6:c.1499C=	ENSP00000389175.2:p.Ala500=
ENST00000461183.5:c.771C=	ENSP00000417264.1:p.Gly257=
ENST00000471180.5:c.642C=	ENSP00000417526.1:p.Gly214=
ENST00000473032.5:c.537C=	ENSP00000418951.1:p.Gly179=
ENST00000486393.5:c.*862C=	ENSP00000419868.1:n.*862C=
ENST00000489173.1:n.1793C=
NM_145262.3:c.1499C=	NP_660305.2:p.Ala500=
NR_026699.1:n.1597C=
NR_026700.1:n.703C=
NR_026701.1:n.1595C=
NR_026702.1:n.633C=
XM_005264878.2:c.*618C=	XP_005264935.1:n.*618C=
XR_245095.2:n.2750C=
XM_017005730.1:c.1118C=	XP_016861219.1:p.Ala373=
XM_024453351.1:c.1499C=	XP_024309119.1:p.Ala500=
XM_024453352.1:c.*618C=	XP_024309120.1:n.*618C=
XR_001740022.2:n.3401C=
XR_001740023.2:n.2925C=
XR_245095.4:n.2751C=
NM_145262.4:c.1499C= MANE Select	NP_660305.2:p.Ala500=
NR_026699.2:n.1589C=
NR_026700.2:n.695C=
NR_026701.2:n.1587C=
NR_026702.2:n.625C=
NM_001144951.2:c.*618C=	NP_001138423.1:n.*618C=