Canonical Allele Identifier: CA433752047

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327150G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293134G>A , CM000665.2:g.52293134G>A	GRCh38
NC_000003.11:g.52327150G>A , CM000665.1:g.52327150G>A	GRCh37
NC_000003.10:g.52302190G>A	NCBI36
NG_023246.1:g.10315G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*8G>A MANE Select	ENSP00000389175.2:n.*8G>A
ENST00000436784.6:c.*8G>A	ENSP00000389175.2:n.*8G>A
ENST00000461183.5:c.852G>A	ENSP00000417264.1:p.Ter284=
ENST00000471180.5:c.723G>A	ENSP00000417526.1:p.Ter241=
ENST00000473032.5:c.618G>A	ENSP00000418951.1:p.Ter206=
ENST00000486393.5:c.*943G>A	ENSP00000419868.1:n.*943G>A
ENST00000489173.1:n.1874G>A
NM_145262.3:c.*8G>A	NP_660305.2:n.*8G>A
NR_026699.1:n.1678G>A
NR_026700.1:n.784G>A
NR_026701.1:n.1676G>A
NR_026702.1:n.714G>A
XM_005264878.2:c.*699G>A	XP_005264935.1:n.*699G>A
XR_245095.2:n.2831G>A
XM_017005730.1:c.*8G>A	XP_016861219.1:n.*8G>A
XM_024453351.1:c.*8G>A	XP_024309119.1:n.*8G>A
XM_024453352.1:c.*699G>A	XP_024309120.1:n.*699G>A
XR_001740022.2:n.3482G>A
XR_001740023.2:n.3006G>A
XR_245095.4:n.2832G>A
NM_145262.4:c.*8G>A MANE Select	NP_660305.2:n.*8G>A
NR_026699.2:n.1670G>A
NR_026700.2:n.776G>A
NR_026701.2:n.1668G>A
NR_026702.2:n.706G>A
NM_001144951.2:c.*699G>A	NP_001138423.1:n.*699G>A