Canonical Allele Identifier: CA353076080

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326962G>C (hg19) ; chr3:g.52292946G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292946G>C , CM000665.2:g.52292946G>C	GRCh38
NC_000003.11:g.52326962G>C , CM000665.1:g.52326962G>C	GRCh37
NC_000003.10:g.52302002G>C	NCBI36
NG_023246.1:g.10127G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1392G>C MANE Select	ENSP00000389175.2:p.Trp464Cys
ENST00000305690.12:c.*511G>C	ENSP00000301965.9:n.*511G>C
ENST00000436784.6:c.1392G>C	ENSP00000389175.2:p.Trp464Cys
ENST00000461183.5:c.764-100G>C	ENSP00000417264.1:n.764-100G>C
ENST00000471180.5:c.635-100G>C	ENSP00000417526.1:n.635-100G>C
ENST00000473032.5:c.530-100G>C	ENSP00000418951.1:n.530-100G>C
ENST00000477382.1:c.*511G>C	ENSP00000419008.1:n.*511G>C
ENST00000486393.5:c.*755G>C	ENSP00000419868.1:n.*755G>C
ENST00000489173.1:n.1686G>C
NM_001144951.1:c.*511G>C	NP_001138423.1:n.*511G>C
NM_145262.3:c.1392G>C	NP_660305.2:p.Trp464Cys
NR_026699.1:n.1490G>C
NR_026700.1:n.696-100G>C
NR_026701.1:n.1488G>C
NR_026702.1:n.626-100G>C
XM_005264878.2:c.*511G>C	XP_005264935.1:n.*511G>C
XR_245095.2:n.2743-100G>C
XM_017005730.1:c.1011G>C	XP_016861219.1:p.Trp337Cys
XM_024453351.1:c.1392G>C	XP_024309119.1:p.Trp464Cys
XM_024453352.1:c.*511G>C	XP_024309120.1:n.*511G>C
XR_001740022.2:n.3294G>C
XR_001740023.2:n.2918-100G>C
XR_245095.4:n.2744-100G>C
NM_145262.4:c.1392G>C MANE Select	NP_660305.2:p.Trp464Cys
NR_026699.2:n.1482G>C
NR_026700.2:n.688-100G>C
NR_026701.2:n.1480G>C
NR_026702.2:n.618-100G>C
NM_001144951.2:c.*511G>C	NP_001138423.1:n.*511G>C