Canonical Allele Identifier: CA353075752

Gene: GLYCTK

Linked Data

• COSMIC: COSM1309324
• MyVariant Identifiers: chr3:g.52326880G>T (hg19) ; chr3:g.52292864G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292864G>T , CM000665.2:g.52292864G>T	GRCh38
NC_000003.11:g.52326880G>T , CM000665.1:g.52326880G>T	GRCh37
NC_000003.10:g.52301920G>T	NCBI36
NG_023246.1:g.10045G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1310G>T MANE Select	ENSP00000389175.2:p.Trp437Leu
ENST00000305690.12:c.*429G>T	ENSP00000301965.9:n.*429G>T
ENST00000436784.6:c.1310G>T	ENSP00000389175.2:p.Trp437Leu
ENST00000461183.5:c.764-182G>T	ENSP00000417264.1:n.764-182G>T
ENST00000471180.5:c.635-182G>T	ENSP00000417526.1:n.635-182G>T
ENST00000473032.5:c.530-182G>T	ENSP00000418951.1:n.530-182G>T
ENST00000477382.1:c.*429G>T	ENSP00000419008.1:n.*429G>T
ENST00000486393.5:c.*673G>T	ENSP00000419868.1:n.*673G>T
ENST00000489173.1:n.1604G>T
NM_001144951.1:c.*429G>T	NP_001138423.1:n.*429G>T
NM_145262.3:c.1310G>T	NP_660305.2:p.Trp437Leu
NR_026699.1:n.1408G>T
NR_026700.1:n.696-182G>T
NR_026701.1:n.1406G>T
NR_026702.1:n.626-182G>T
XM_005264878.2:c.*429G>T	XP_005264935.1:n.*429G>T
XR_245095.2:n.2743-182G>T
XM_017005730.1:c.929G>T	XP_016861219.1:p.Trp310Leu
XM_024453351.1:c.1310G>T	XP_024309119.1:p.Trp437Leu
XM_024453352.1:c.*429G>T	XP_024309120.1:n.*429G>T
XR_001740022.2:n.3212G>T
XR_001740023.2:n.2918-182G>T
XR_245095.4:n.2744-182G>T
NM_145262.4:c.1310G>T MANE Select	NP_660305.2:p.Trp437Leu
NR_026699.2:n.1400G>T
NR_026700.2:n.688-182G>T
NR_026701.2:n.1398G>T
NR_026702.2:n.618-182G>T
NM_001144951.2:c.*429G>T	NP_001138423.1:n.*429G>T