Canonical Allele Identifier: CA1364789264

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293122G= , CM000665.2:g.52293122G=	GRCh38
NC_000003.11:g.52327138G= , CM000665.1:g.52327138G=	GRCh37
NC_000003.10:g.52302178G=	NCBI36
NG_023246.1:g.10303G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1568G= MANE Select	ENSP00000389175.2:p.Arg523=
ENST00000436784.6:c.1568G=	ENSP00000389175.2:p.Arg523=
ENST00000461183.5:c.840G=	ENSP00000417264.1:p.Ser280=
ENST00000471180.5:c.711G=	ENSP00000417526.1:p.Ser237=
ENST00000473032.5:c.606G=	ENSP00000418951.1:p.Ser202=
ENST00000486393.5:c.*931G=	ENSP00000419868.1:n.*931G=
ENST00000489173.1:n.1862G=
NM_145262.3:c.1568G=	NP_660305.2:p.Arg523=
NR_026699.1:n.1666G=
NR_026700.1:n.772G=
NR_026701.1:n.1664G=
NR_026702.1:n.702G=
XM_005264878.2:c.*687G=	XP_005264935.1:n.*687G=
XR_245095.2:n.2819G=
XM_017005730.1:c.1187G=	XP_016861219.1:p.Arg396=
XM_024453351.1:c.1568G=	XP_024309119.1:p.Arg523=
XM_024453352.1:c.*687G=	XP_024309120.1:n.*687G=
XR_001740022.2:n.3470G=
XR_001740023.2:n.2994G=
XR_245095.4:n.2820G=
NM_145262.4:c.1568G= MANE Select	NP_660305.2:p.Arg523=
NR_026699.2:n.1658G=
NR_026700.2:n.764G=
NR_026701.2:n.1656G=
NR_026702.2:n.694G=
NM_001144951.2:c.*687G=	NP_001138423.1:n.*687G=