Canonical Allele Identifier: CA433752051

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327152T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293136T>A , CM000665.2:g.52293136T>A	GRCh38
NC_000003.11:g.52327152T>A , CM000665.1:g.52327152T>A	GRCh37
NC_000003.10:g.52302192T>A	NCBI36
NG_023246.1:g.10317T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.*10T>A MANE Select	ENSP00000389175.2:n.*10T>A
ENST00000436784.6:c.*10T>A	ENSP00000389175.2:n.*10T>A
ENST00000461183.5:c.*2T>A	ENSP00000417264.1:n.*2T>A
ENST00000471180.5:c.*2T>A	ENSP00000417526.1:n.*2T>A
ENST00000473032.5:c.*2T>A	ENSP00000418951.1:n.*2T>A
ENST00000486393.5:c.*945T>A	ENSP00000419868.1:n.*945T>A
ENST00000489173.1:n.1876T>A
NM_145262.3:c.*10T>A	NP_660305.2:n.*10T>A
NR_026699.1:n.1680T>A
NR_026700.1:n.786T>A
NR_026701.1:n.1678T>A
NR_026702.1:n.716T>A
XM_005264878.2:c.*701T>A	XP_005264935.1:n.*701T>A
XR_245095.2:n.2833T>A
XM_017005730.1:c.*10T>A	XP_016861219.1:n.*10T>A
XM_024453351.1:c.*10T>A	XP_024309119.1:n.*10T>A
XM_024453352.1:c.*701T>A	XP_024309120.1:n.*701T>A
XR_001740022.2:n.3484T>A
XR_001740023.2:n.3008T>A
XR_245095.4:n.2834T>A
NM_145262.4:c.*10T>A MANE Select	NP_660305.2:n.*10T>A
NR_026699.2:n.1672T>A
NR_026700.2:n.778T>A
NR_026701.2:n.1670T>A
NR_026702.2:n.708T>A
NM_001144951.2:c.*701T>A	NP_001138423.1:n.*701T>A