Canonical Allele Identifier: CA2665985173

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293265-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293265C>G , CM000665.2:g.52293265C>G	GRCh38
NC_000003.11:g.52327281C>G , CM000665.1:g.52327281C>G	GRCh37
NC_000003.10:g.52302321C>G	NCBI36
NG_023246.1:g.10446C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*139C>G MANE Select	ENSP00000389175.2:n.*139C>G
ENST00000436784.6:c.*139C>G	ENSP00000389175.2:n.*139C>G
ENST00000471180.5:c.*59-42C>G	ENSP00000417526.1:n.*59-42C>G
ENST00000473032.5:c.*59-42C>G	ENSP00000418951.1:n.*59-42C>G
ENST00000486393.5:c.*1074C>G	ENSP00000419868.1:n.*1074C>G
ENST00000489173.1:n.1915-42C>G
NM_145262.3:c.*139C>G	NP_660305.2:n.*139C>G
NR_026699.1:n.1809C>G
NR_026700.1:n.843-42C>G
NR_026701.1:n.1735-42C>G
NR_026702.1:n.773-42C>G
XM_005264878.2:c.*830C>G	XP_005264935.1:n.*830C>G
XR_245095.2:n.2890-42C>G
XM_017005730.1:c.*139C>G	XP_016861219.1:n.*139C>G
XM_024453351.1:c.*139C>G	XP_024309119.1:n.*139C>G
XM_024453352.1:c.*830C>G	XP_024309120.1:n.*830C>G
XR_001740022.2:n.3541-42C>G
XR_001740023.2:n.3065-42C>G
XR_245095.4:n.2891-42C>G
NM_145262.4:c.*139C>G MANE Select	NP_660305.2:n.*139C>G
NR_026699.2:n.1801C>G
NR_026700.2:n.835-42C>G
NR_026701.2:n.1727-42C>G
NR_026702.2:n.765-42C>G
NM_001144951.2:c.*830C>G	NP_001138423.1:n.*830C>G