Canonical Allele Identifier: CA2756266620

Gene: GLYCTK

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293312C>G , CM000665.2:g.52293312C>G	GRCh38
NC_000003.11:g.52327328C>G , CM000665.1:g.52327328C>G	GRCh37
NC_000003.10:g.52302368C>G	NCBI36
NG_023246.1:g.10493C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*186C>G MANE Select	ENSP00000389175.2:n.*186C>G
ENST00000436784.6:c.*186C>G	ENSP00000389175.2:n.*186C>G
ENST00000471180.5:c.*64C>G	ENSP00000417526.1:n.*64C>G
ENST00000473032.5:c.*64C>G	ENSP00000418951.1:n.*64C>G
ENST00000486393.5:c.*1121C>G	ENSP00000419868.1:n.*1121C>G
ENST00000489173.1:n.1920C>G
NM_145262.3:c.*186C>G	NP_660305.2:n.*186C>G
NR_026699.1:n.1856C>G
NR_026700.1:n.848C>G
NR_026701.1:n.1740C>G
NR_026702.1:n.778C>G
XM_005264878.2:c.*877C>G	XP_005264935.1:n.*877C>G
XR_245095.2:n.2895C>G
XM_017005730.1:c.*186C>G	XP_016861219.1:n.*186C>G
XM_024453351.1:c.*186C>G	XP_024309119.1:n.*186C>G
XM_024453352.1:c.*877C>G	XP_024309120.1:n.*877C>G
XR_001740022.2:n.3546C>G
XR_001740023.2:n.3070C>G
XR_245095.4:n.2896C>G
NM_145262.4:c.*186C>G MANE Select	NP_660305.2:n.*186C>G
NR_026699.2:n.1848C>G
NR_026700.2:n.840C>G
NR_026701.2:n.1732C>G
NR_026702.2:n.770C>G
NM_001144951.2:c.*877C>G	NP_001138423.1:n.*877C>G