Canonical Allele Identifier: CA353075993

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326940C>G (hg19) ; chr3:g.52292924C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292924C>G , CM000665.2:g.52292924C>G	GRCh38
NC_000003.11:g.52326940C>G , CM000665.1:g.52326940C>G	GRCh37
NC_000003.10:g.52301980C>G	NCBI36
NG_023246.1:g.10105C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1370C>G MANE Select	ENSP00000389175.2:p.Pro457Arg
ENST00000305690.12:c.*489C>G	ENSP00000301965.9:n.*489C>G
ENST00000436784.6:c.1370C>G	ENSP00000389175.2:p.Pro457Arg
ENST00000461183.5:c.764-122C>G	ENSP00000417264.1:n.764-122C>G
ENST00000471180.5:c.635-122C>G	ENSP00000417526.1:n.635-122C>G
ENST00000473032.5:c.530-122C>G	ENSP00000418951.1:n.530-122C>G
ENST00000477382.1:c.*489C>G	ENSP00000419008.1:n.*489C>G
ENST00000486393.5:c.*733C>G	ENSP00000419868.1:n.*733C>G
ENST00000489173.1:n.1664C>G
NM_001144951.1:c.*489C>G	NP_001138423.1:n.*489C>G
NM_145262.3:c.1370C>G	NP_660305.2:p.Pro457Arg
NR_026699.1:n.1468C>G
NR_026700.1:n.696-122C>G
NR_026701.1:n.1466C>G
NR_026702.1:n.626-122C>G
XM_005264878.2:c.*489C>G	XP_005264935.1:n.*489C>G
XR_245095.2:n.2743-122C>G
XM_017005730.1:c.989C>G	XP_016861219.1:p.Pro330Arg
XM_024453351.1:c.1370C>G	XP_024309119.1:p.Pro457Arg
XM_024453352.1:c.*489C>G	XP_024309120.1:n.*489C>G
XR_001740022.2:n.3272C>G
XR_001740023.2:n.2918-122C>G
XR_245095.4:n.2744-122C>G
NM_145262.4:c.1370C>G MANE Select	NP_660305.2:p.Pro457Arg
NR_026699.2:n.1460C>G
NR_026700.2:n.688-122C>G
NR_026701.2:n.1458C>G
NR_026702.2:n.618-122C>G
NM_001144951.2:c.*489C>G	NP_001138423.1:n.*489C>G