Canonical Allele Identifier: CA433752061

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327155C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293139C>G , CM000665.2:g.52293139C>G	GRCh38
NC_000003.11:g.52327155C>G , CM000665.1:g.52327155C>G	GRCh37
NC_000003.10:g.52302195C>G	NCBI36
NG_023246.1:g.10320C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.*13C>G MANE Select	ENSP00000389175.2:n.*13C>G
ENST00000436784.6:c.*13C>G	ENSP00000389175.2:n.*13C>G
ENST00000461183.5:c.*5C>G	ENSP00000417264.1:n.*5C>G
ENST00000471180.5:c.*5C>G	ENSP00000417526.1:n.*5C>G
ENST00000473032.5:c.*5C>G	ENSP00000418951.1:n.*5C>G
ENST00000486393.5:c.*948C>G	ENSP00000419868.1:n.*948C>G
ENST00000489173.1:n.1879C>G
NM_145262.3:c.*13C>G	NP_660305.2:n.*13C>G
NR_026699.1:n.1683C>G
NR_026700.1:n.789C>G
NR_026701.1:n.1681C>G
NR_026702.1:n.719C>G
XM_005264878.2:c.*704C>G	XP_005264935.1:n.*704C>G
XR_245095.2:n.2836C>G
XM_017005730.1:c.*13C>G	XP_016861219.1:n.*13C>G
XM_024453351.1:c.*13C>G	XP_024309119.1:n.*13C>G
XM_024453352.1:c.*704C>G	XP_024309120.1:n.*704C>G
XR_001740022.2:n.3487C>G
XR_001740023.2:n.3011C>G
XR_245095.4:n.2837C>G
NM_145262.4:c.*13C>G MANE Select	NP_660305.2:n.*13C>G
NR_026699.2:n.1675C>G
NR_026700.2:n.781C>G
NR_026701.2:n.1673C>G
NR_026702.2:n.711C>G
NM_001144951.2:c.*704C>G	NP_001138423.1:n.*704C>G