Canonical Allele Identifier: CA2581874838

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293290T>A , CM000665.2:g.52293290T>A	GRCh38
NC_000003.11:g.52327306T>A , CM000665.1:g.52327306T>A	GRCh37
NC_000003.10:g.52302346T>A	NCBI36
NG_023246.1:g.10471T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*164T>A MANE Select	ENSP00000389175.2:n.*164T>A
ENST00000436784.6:c.*164T>A	ENSP00000389175.2:n.*164T>A
ENST00000471180.5:c.*59-17T>A	ENSP00000417526.1:n.*59-17T>A
ENST00000473032.5:c.*59-17T>A	ENSP00000418951.1:n.*59-17T>A
ENST00000486393.5:c.*1099T>A	ENSP00000419868.1:n.*1099T>A
ENST00000489173.1:n.1915-17T>A
NM_145262.3:c.*164T>A	NP_660305.2:n.*164T>A
NR_026699.1:n.1834T>A
NR_026700.1:n.843-17T>A
NR_026701.1:n.1735-17T>A
NR_026702.1:n.773-17T>A
XM_005264878.2:c.*855T>A	XP_005264935.1:n.*855T>A
XR_245095.2:n.2890-17T>A
XM_017005730.1:c.*164T>A	XP_016861219.1:n.*164T>A
XM_024453351.1:c.*164T>A	XP_024309119.1:n.*164T>A
XM_024453352.1:c.*855T>A	XP_024309120.1:n.*855T>A
XR_001740022.2:n.3541-17T>A
XR_001740023.2:n.3065-17T>A
XR_245095.4:n.2891-17T>A
NM_145262.4:c.*164T>A MANE Select	NP_660305.2:n.*164T>A
NR_026699.2:n.1826T>A
NR_026700.2:n.835-17T>A
NR_026701.2:n.1727-17T>A
NR_026702.2:n.765-17T>A
NM_001144951.2:c.*855T>A	NP_001138423.1:n.*855T>A