Canonical Allele Identifier: CA433752025

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327037A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293021A>G , CM000665.2:g.52293021A>G	GRCh38
NC_000003.11:g.52327037A>G , CM000665.1:g.52327037A>G	GRCh37
NC_000003.10:g.52302077A>G	NCBI36
NG_023246.1:g.10202A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1467A>G MANE Select	ENSP00000389175.2:p.Ser489=
ENST00000436784.6:c.1467A>G	ENSP00000389175.2:p.Ser489=
ENST00000461183.5:c.764-25A>G	ENSP00000417264.1:n.764-25A>G
ENST00000471180.5:c.635-25A>G	ENSP00000417526.1:n.635-25A>G
ENST00000473032.5:c.530-25A>G	ENSP00000418951.1:n.530-25A>G
ENST00000486393.5:c.*830A>G	ENSP00000419868.1:n.*830A>G
ENST00000489173.1:n.1761A>G
NM_145262.3:c.1467A>G	NP_660305.2:p.Ser489=
NR_026699.1:n.1565A>G
NR_026700.1:n.696-25A>G
NR_026701.1:n.1563A>G
NR_026702.1:n.626-25A>G
XM_005264878.2:c.*586A>G	XP_005264935.1:n.*586A>G
XR_245095.2:n.2743-25A>G
XM_017005730.1:c.1086A>G	XP_016861219.1:p.Ser362=
XM_024453351.1:c.1467A>G	XP_024309119.1:p.Ser489=
XM_024453352.1:c.*586A>G	XP_024309120.1:n.*586A>G
XR_001740022.2:n.3369A>G
XR_001740023.2:n.2918-25A>G
XR_245095.4:n.2744-25A>G
NM_145262.4:c.1467A>G MANE Select	NP_660305.2:p.Ser489=
NR_026699.2:n.1557A>G
NR_026700.2:n.688-25A>G
NR_026701.2:n.1555A>G
NR_026702.2:n.618-25A>G
NM_001144951.2:c.*586A>G	NP_001138423.1:n.*586A>G