Canonical Allele Identifier: CA353076983

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327146C>G (hg19) ; chr3:g.52293130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293130C>G , CM000665.2:g.52293130C>G	GRCh38
NC_000003.11:g.52327146C>G , CM000665.1:g.52327146C>G	GRCh37
NC_000003.10:g.52302186C>G	NCBI36
NG_023246.1:g.10311C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*4C>G MANE Select	ENSP00000389175.2:n.*4C>G
ENST00000436784.6:c.*4C>G	ENSP00000389175.2:n.*4C>G
ENST00000461183.5:c.848C>G	ENSP00000417264.1:p.Ala283Gly
ENST00000471180.5:c.719C>G	ENSP00000417526.1:p.Ala240Gly
ENST00000473032.5:c.614C>G	ENSP00000418951.1:p.Ala205Gly
ENST00000486393.5:c.*939C>G	ENSP00000419868.1:n.*939C>G
ENST00000489173.1:n.1870C>G
NM_145262.3:c.*4C>G	NP_660305.2:n.*4C>G
NR_026699.1:n.1674C>G
NR_026700.1:n.780C>G
NR_026701.1:n.1672C>G
NR_026702.1:n.710C>G
XM_005264878.2:c.*695C>G	XP_005264935.1:n.*695C>G
XR_245095.2:n.2827C>G
XM_017005730.1:c.*4C>G	XP_016861219.1:n.*4C>G
XM_024453351.1:c.*4C>G	XP_024309119.1:n.*4C>G
XM_024453352.1:c.*695C>G	XP_024309120.1:n.*695C>G
XR_001740022.2:n.3478C>G
XR_001740023.2:n.3002C>G
XR_245095.4:n.2828C>G
NM_145262.4:c.*4C>G MANE Select	NP_660305.2:n.*4C>G
NR_026699.2:n.1666C>G
NR_026700.2:n.772C>G
NR_026701.2:n.1664C>G
NR_026702.2:n.702C>G
NM_001144951.2:c.*695C>G	NP_001138423.1:n.*695C>G