Canonical Allele Identifier: CA1364789249

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293093G= , CM000665.2:g.52293093G=	GRCh38
NC_000003.11:g.52327109G= , CM000665.1:g.52327109G=	GRCh37
NC_000003.10:g.52302149G=	NCBI36
NG_023246.1:g.10274G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1539G= MANE Select	ENSP00000389175.2:p.Met513=
ENST00000436784.6:c.1539G=	ENSP00000389175.2:p.Met513=
ENST00000461183.5:c.811G=	ENSP00000417264.1:p.Gly271=
ENST00000471180.5:c.682G=	ENSP00000417526.1:p.Gly228=
ENST00000473032.5:c.577G=	ENSP00000418951.1:p.Gly193=
ENST00000486393.5:c.*902G=	ENSP00000419868.1:n.*902G=
ENST00000489173.1:n.1833G=
NM_145262.3:c.1539G=	NP_660305.2:p.Met513=
NR_026699.1:n.1637G=
NR_026700.1:n.743G=
NR_026701.1:n.1635G=
NR_026702.1:n.673G=
XM_005264878.2:c.*658G=	XP_005264935.1:n.*658G=
XR_245095.2:n.2790G=
XM_017005730.1:c.1158G=	XP_016861219.1:p.Met386=
XM_024453351.1:c.1539G=	XP_024309119.1:p.Met513=
XM_024453352.1:c.*658G=	XP_024309120.1:n.*658G=
XR_001740022.2:n.3441G=
XR_001740023.2:n.2965G=
XR_245095.4:n.2791G=
NM_145262.4:c.1539G= MANE Select	NP_660305.2:p.Met513=
NR_026699.2:n.1629G=
NR_026700.2:n.735G=
NR_026701.2:n.1627G=
NR_026702.2:n.665G=
NM_001144951.2:c.*658G=	NP_001138423.1:n.*658G=