Canonical Allele Identifier: CA433752044
Gene: GLYCTK HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.52327141G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52293125G>A , CM000665.2:g.52293125G>A GRCh38
NC_000003.11:g.52327141G>A , CM000665.1:g.52327141G>A GRCh37
NC_000003.10:g.52302181G>A NCBI36
NG_023246.1:g.10306G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000436784.7:c.1571G>A MANE Select ENSP00000389175.2:p.Ter524=
ENST00000436784.6:c.1571G>A ENSP00000389175.2:p.Ter524=
ENST00000461183.5:c.843G>A ENSP00000417264.1:p.Val281=
ENST00000471180.5:c.714G>A ENSP00000417526.1:p.Val238=
ENST00000473032.5:c.609G>A ENSP00000418951.1:p.Val203=
ENST00000486393.5:c.*934G>A ENSP00000419868.1:n.*934G>A
ENST00000489173.1:n.1865G>A
NM_145262.3:c.1571G>A NP_660305.2:p.Ter524=
NR_026699.1:n.1669G>A
NR_026700.1:n.775G>A
NR_026701.1:n.1667G>A
NR_026702.1:n.705G>A
XM_005264878.2:c.*690G>A XP_005264935.1:n.*690G>A
XR_245095.2:n.2822G>A
XM_017005730.1:c.1190G>A XP_016861219.1:p.Ter397=
XM_024453351.1:c.1571G>A XP_024309119.1:p.Ter524=
XM_024453352.1:c.*690G>A XP_024309120.1:n.*690G>A
XR_001740022.2:n.3473G>A
XR_001740023.2:n.2997G>A
XR_245095.4:n.2823G>A
NM_145262.4:c.1571G>A MANE Select NP_660305.2:p.Ter524=
NR_026699.2:n.1661G>A
NR_026700.2:n.767G>A
NR_026701.2:n.1659G>A
NR_026702.2:n.697G>A
NM_001144951.2:c.*690G>A NP_001138423.1:n.*690G>A