Canonical Allele Identifier: CA353076663

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327089A>G (hg19) ; chr3:g.52293073A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293073A>G , CM000665.2:g.52293073A>G	GRCh38
NC_000003.11:g.52327089A>G , CM000665.1:g.52327089A>G	GRCh37
NC_000003.10:g.52302129A>G	NCBI36
NG_023246.1:g.10254A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1519A>G MANE Select	ENSP00000389175.2:p.Met507Val
ENST00000436784.6:c.1519A>G	ENSP00000389175.2:p.Met507Val
ENST00000461183.5:c.791A>G	ENSP00000417264.1:p.Asp264Gly
ENST00000471180.5:c.662A>G	ENSP00000417526.1:p.Asp221Gly
ENST00000473032.5:c.557A>G	ENSP00000418951.1:p.Asp186Gly
ENST00000486393.5:c.*882A>G	ENSP00000419868.1:n.*882A>G
ENST00000489173.1:n.1813A>G
NM_145262.3:c.1519A>G	NP_660305.2:p.Met507Val
NR_026699.1:n.1617A>G
NR_026700.1:n.723A>G
NR_026701.1:n.1615A>G
NR_026702.1:n.653A>G
XM_005264878.2:c.*638A>G	XP_005264935.1:n.*638A>G
XR_245095.2:n.2770A>G
XM_017005730.1:c.1138A>G	XP_016861219.1:p.Met380Val
XM_024453351.1:c.1519A>G	XP_024309119.1:p.Met507Val
XM_024453352.1:c.*638A>G	XP_024309120.1:n.*638A>G
XR_001740022.2:n.3421A>G
XR_001740023.2:n.2945A>G
XR_245095.4:n.2771A>G
NM_145262.4:c.1519A>G MANE Select	NP_660305.2:p.Met507Val
NR_026699.2:n.1609A>G
NR_026700.2:n.715A>G
NR_026701.2:n.1607A>G
NR_026702.2:n.645A>G
NM_001144951.2:c.*638A>G	NP_001138423.1:n.*638A>G