Canonical Allele Identifier: CA353076618

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52327078T>G (hg19) ; chr3:g.52293062T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293062T>G , CM000665.2:g.52293062T>G	GRCh38
NC_000003.11:g.52327078T>G , CM000665.1:g.52327078T>G	GRCh37
NC_000003.10:g.52302118T>G	NCBI36
NG_023246.1:g.10243T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1508T>G MANE Select	ENSP00000389175.2:p.Leu503Arg
ENST00000436784.6:c.1508T>G	ENSP00000389175.2:p.Leu503Arg
ENST00000461183.5:c.780T>G	ENSP00000417264.1:p.Ala260=
ENST00000471180.5:c.651T>G	ENSP00000417526.1:p.Ala217=
ENST00000473032.5:c.546T>G	ENSP00000418951.1:p.Ala182=
ENST00000486393.5:c.*871T>G	ENSP00000419868.1:n.*871T>G
ENST00000489173.1:n.1802T>G
NM_145262.3:c.1508T>G	NP_660305.2:p.Leu503Arg
NR_026699.1:n.1606T>G
NR_026700.1:n.712T>G
NR_026701.1:n.1604T>G
NR_026702.1:n.642T>G
XM_005264878.2:c.*627T>G	XP_005264935.1:n.*627T>G
XR_245095.2:n.2759T>G
XM_017005730.1:c.1127T>G	XP_016861219.1:p.Leu376Arg
XM_024453351.1:c.1508T>G	XP_024309119.1:p.Leu503Arg
XM_024453352.1:c.*627T>G	XP_024309120.1:n.*627T>G
XR_001740022.2:n.3410T>G
XR_001740023.2:n.2934T>G
XR_245095.4:n.2760T>G
NM_145262.4:c.1508T>G MANE Select	NP_660305.2:p.Leu503Arg
NR_026699.2:n.1598T>G
NR_026700.2:n.704T>G
NR_026701.2:n.1596T>G
NR_026702.2:n.634T>G
NM_001144951.2:c.*627T>G	NP_001138423.1:n.*627T>G