Canonical Allele Identifier: CA1364789265

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293123G= , CM000665.2:g.52293123G=	GRCh38
NC_000003.11:g.52327139G= , CM000665.1:g.52327139G=	GRCh37
NC_000003.10:g.52302179G=	NCBI36
NG_023246.1:g.10304G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1569G= MANE Select	ENSP00000389175.2:p.Arg523=
ENST00000436784.6:c.1569G=	ENSP00000389175.2:p.Arg523=
ENST00000461183.5:c.841G=	ENSP00000417264.1:p.Val281=
ENST00000471180.5:c.712G=	ENSP00000417526.1:p.Val238=
ENST00000473032.5:c.607G=	ENSP00000418951.1:p.Val203=
ENST00000486393.5:c.*932G=	ENSP00000419868.1:n.*932G=
ENST00000489173.1:n.1863G=
NM_145262.3:c.1569G=	NP_660305.2:p.Arg523=
NR_026699.1:n.1667G=
NR_026700.1:n.773G=
NR_026701.1:n.1665G=
NR_026702.1:n.703G=
XM_005264878.2:c.*688G=	XP_005264935.1:n.*688G=
XR_245095.2:n.2820G=
XM_017005730.1:c.1188G=	XP_016861219.1:p.Arg396=
XM_024453351.1:c.1569G=	XP_024309119.1:p.Arg523=
XM_024453352.1:c.*688G=	XP_024309120.1:n.*688G=
XR_001740022.2:n.3471G=
XR_001740023.2:n.2995G=
XR_245095.4:n.2821G=
NM_145262.4:c.1569G= MANE Select	NP_660305.2:p.Arg523=
NR_026699.2:n.1659G=
NR_026700.2:n.765G=
NR_026701.2:n.1657G=
NR_026702.2:n.695G=
NM_001144951.2:c.*688G=	NP_001138423.1:n.*688G=