Canonical Allele Identifier: CA433882967

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326968A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292952A>C , CM000665.2:g.52292952A>C	GRCh38
NC_000003.11:g.52326968A>C , CM000665.1:g.52326968A>C	GRCh37
NC_000003.10:g.52302008A>C	NCBI36
NG_023246.1:g.10133A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1398A>C MANE Select	ENSP00000389175.2:p.Thr466=
ENST00000305690.12:c.*517A>C	ENSP00000301965.9:n.*517A>C
ENST00000436784.6:c.1398A>C	ENSP00000389175.2:p.Thr466=
ENST00000461183.5:c.764-94A>C	ENSP00000417264.1:n.764-94A>C
ENST00000471180.5:c.635-94A>C	ENSP00000417526.1:n.635-94A>C
ENST00000473032.5:c.530-94A>C	ENSP00000418951.1:n.530-94A>C
ENST00000477382.1:c.*517A>C	ENSP00000419008.1:n.*517A>C
ENST00000486393.5:c.*761A>C	ENSP00000419868.1:n.*761A>C
ENST00000489173.1:n.1692A>C
NM_001144951.1:c.*517A>C	NP_001138423.1:n.*517A>C
NM_145262.3:c.1398A>C	NP_660305.2:p.Thr466=
NR_026699.1:n.1496A>C
NR_026700.1:n.696-94A>C
NR_026701.1:n.1494A>C
NR_026702.1:n.626-94A>C
XM_005264878.2:c.*517A>C	XP_005264935.1:n.*517A>C
XR_245095.2:n.2743-94A>C
XM_017005730.1:c.1017A>C	XP_016861219.1:p.Thr339=
XM_024453351.1:c.1398A>C	XP_024309119.1:p.Thr466=
XM_024453352.1:c.*517A>C	XP_024309120.1:n.*517A>C
XR_001740022.2:n.3300A>C
XR_001740023.2:n.2918-94A>C
XR_245095.4:n.2744-94A>C
NM_145262.4:c.1398A>C MANE Select	NP_660305.2:p.Thr466=
NR_026699.2:n.1488A>C
NR_026700.2:n.688-94A>C
NR_026701.2:n.1486A>C
NR_026702.2:n.618-94A>C
NM_001144951.2:c.*517A>C	NP_001138423.1:n.*517A>C