Canonical Allele Identifier: CA353075728

Gene: GLYCTK

Linked Data

• MyVariant Identifiers: chr3:g.52326874G>T (hg19) ; chr3:g.52292858G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52292858G>T , CM000665.2:g.52292858G>T	GRCh38
NC_000003.11:g.52326874G>T , CM000665.1:g.52326874G>T	GRCh37
NC_000003.10:g.52301914G>T	NCBI36
NG_023246.1:g.10039G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1304G>T MANE Select	ENSP00000389175.2:p.Arg435Ile
ENST00000305690.12:c.*423G>T	ENSP00000301965.9:n.*423G>T
ENST00000436784.6:c.1304G>T	ENSP00000389175.2:p.Arg435Ile
ENST00000461183.5:c.764-188G>T	ENSP00000417264.1:n.764-188G>T
ENST00000471180.5:c.635-188G>T	ENSP00000417526.1:n.635-188G>T
ENST00000473032.5:c.530-188G>T	ENSP00000418951.1:n.530-188G>T
ENST00000477382.1:c.*423G>T	ENSP00000419008.1:n.*423G>T
ENST00000486393.5:c.*667G>T	ENSP00000419868.1:n.*667G>T
ENST00000489173.1:n.1598G>T
NM_001144951.1:c.*423G>T	NP_001138423.1:n.*423G>T
NM_145262.3:c.1304G>T	NP_660305.2:p.Arg435Ile
NR_026699.1:n.1402G>T
NR_026700.1:n.696-188G>T
NR_026701.1:n.1400G>T
NR_026702.1:n.626-188G>T
XM_005264878.2:c.*423G>T	XP_005264935.1:n.*423G>T
XR_245095.2:n.2743-188G>T
XM_017005730.1:c.923G>T	XP_016861219.1:p.Arg308Ile
XM_024453351.1:c.1304G>T	XP_024309119.1:p.Arg435Ile
XM_024453352.1:c.*423G>T	XP_024309120.1:n.*423G>T
XR_001740022.2:n.3206G>T
XR_001740023.2:n.2918-188G>T
XR_245095.4:n.2744-188G>T
NM_145262.4:c.1304G>T MANE Select	NP_660305.2:p.Arg435Ile
NR_026699.2:n.1394G>T
NR_026700.2:n.688-188G>T
NR_026701.2:n.1392G>T
NR_026702.2:n.618-188G>T
NM_001144951.2:c.*423G>T	NP_001138423.1:n.*423G>T