Canonical Allele Identifier: CA2431983
Gene: GLYCTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52290406C>T , CM000665.2:g.52290406C>T GRCh38
NC_000003.11:g.52324422C>T , CM000665.1:g.52324422C>T GRCh37
NC_000003.10:g.52299462C>T NCBI36
NG_023246.1:g.7587C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.64C>T MANE Select ENSP00000389175.2:p.Arg22Trp
ENST00000305690.12:c.64C>T ENSP00000301965.9:p.Arg22Trp
ENST00000436784.6:c.64C>T ENSP00000389175.2:p.Arg22Trp
ENST00000461183.5:c.126-554C>T ENSP00000417264.1:n.126-554C>T
ENST00000471180.5:c.-4-554C>T ENSP00000417526.1:n.-4-554C>T
ENST00000473032.5:c.64C>T ENSP00000418951.1:p.Arg22Trp
ENST00000473583.1:n.333C>T
ENST00000477382.1:c.64C>T ENSP00000419008.1:p.Arg22Trp
ENST00000486393.5:c.64C>T ENSP00000419868.1:p.Arg22Trp
NM_001144951.1:c.64C>T NP_001138423.1:p.Arg22Trp
NM_145262.3:c.64C>T NP_660305.2:p.Arg22Trp
NR_026699.1:n.160C>T
NR_026700.1:n.58-554C>T
NR_026701.1:n.160C>T
NR_026702.1:n.160C>T
XM_005264878.2:c.64C>T XP_005264935.1:p.Arg22Trp
XR_245095.2:n.1967C>T
XM_017005730.1:c.-4-554C>T XP_016861219.1:n.-4-554C>T
XM_024453351.1:c.64C>T XP_024309119.1:p.Arg22Trp
XM_024453352.1:c.64C>T XP_024309120.1:p.Arg22Trp
XR_001740022.2:n.1966C>T
XR_001740023.2:n.1966C>T
XR_245095.4:n.1968C>T
NM_145262.4:c.64C>T MANE Select NP_660305.2:p.Arg22Trp
NR_026699.2:n.152C>T
NR_026700.2:n.50-554C>T
NR_026701.2:n.152C>T
NR_026702.2:n.152C>T
NM_001144951.2:c.64C>T NP_001138423.1:p.Arg22Trp