Canonical Allele Identifier: CA353076814

Gene: GLYCTK

Linked Data

• COSMIC: COSM1726984
• MyVariant Identifiers: chr3:g.52327117A>G (hg19) ; chr3:g.52293101A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293101A>G , CM000665.2:g.52293101A>G	GRCh38
NC_000003.11:g.52327117A>G , CM000665.1:g.52327117A>G	GRCh37
NC_000003.10:g.52302157A>G	NCBI36
NG_023246.1:g.10282A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1547A>G MANE Select	ENSP00000389175.2:p.His516Arg
ENST00000436784.6:c.1547A>G	ENSP00000389175.2:p.His516Arg
ENST00000461183.5:c.819A>G	ENSP00000417264.1:p.Pro273=
ENST00000471180.5:c.690A>G	ENSP00000417526.1:p.Pro230=
ENST00000473032.5:c.585A>G	ENSP00000418951.1:p.Pro195=
ENST00000486393.5:c.*910A>G	ENSP00000419868.1:n.*910A>G
ENST00000489173.1:n.1841A>G
NM_145262.3:c.1547A>G	NP_660305.2:p.His516Arg
NR_026699.1:n.1645A>G
NR_026700.1:n.751A>G
NR_026701.1:n.1643A>G
NR_026702.1:n.681A>G
XM_005264878.2:c.*666A>G	XP_005264935.1:n.*666A>G
XR_245095.2:n.2798A>G
XM_017005730.1:c.1166A>G	XP_016861219.1:p.His389Arg
XM_024453351.1:c.1547A>G	XP_024309119.1:p.His516Arg
XM_024453352.1:c.*666A>G	XP_024309120.1:n.*666A>G
XR_001740022.2:n.3449A>G
XR_001740023.2:n.2973A>G
XR_245095.4:n.2799A>G
NM_145262.4:c.1547A>G MANE Select	NP_660305.2:p.His516Arg
NR_026699.2:n.1637A>G
NR_026700.2:n.743A>G
NR_026701.2:n.1635A>G
NR_026702.2:n.673A>G
NM_001144951.2:c.*666A>G	NP_001138423.1:n.*666A>G