Canonical Allele Identifier: CA353076443

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293026-C-T
• MyVariant Identifiers: chr3:g.52327042C>T (hg19) ; chr3:g.52293026C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293026C>T , CM000665.2:g.52293026C>T	GRCh38
NC_000003.11:g.52327042C>T , CM000665.1:g.52327042C>T	GRCh37
NC_000003.10:g.52302082C>T	NCBI36
NG_023246.1:g.10207C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.1472C>T MANE Select	ENSP00000389175.2:p.Thr491Ile
ENST00000436784.6:c.1472C>T	ENSP00000389175.2:p.Thr491Ile
ENST00000461183.5:c.764-20C>T	ENSP00000417264.1:n.764-20C>T
ENST00000471180.5:c.635-20C>T	ENSP00000417526.1:n.635-20C>T
ENST00000473032.5:c.530-20C>T	ENSP00000418951.1:n.530-20C>T
ENST00000486393.5:c.*835C>T	ENSP00000419868.1:n.*835C>T
ENST00000489173.1:n.1766C>T
NM_145262.3:c.1472C>T	NP_660305.2:p.Thr491Ile
NR_026699.1:n.1570C>T
NR_026700.1:n.696-20C>T
NR_026701.1:n.1568C>T
NR_026702.1:n.626-20C>T
XM_005264878.2:c.*591C>T	XP_005264935.1:n.*591C>T
XR_245095.2:n.2743-20C>T
XM_017005730.1:c.1091C>T	XP_016861219.1:p.Thr364Ile
XM_024453351.1:c.1472C>T	XP_024309119.1:p.Thr491Ile
XM_024453352.1:c.*591C>T	XP_024309120.1:n.*591C>T
XR_001740022.2:n.3374C>T
XR_001740023.2:n.2918-20C>T
XR_245095.4:n.2744-20C>T
NM_145262.4:c.1472C>T MANE Select	NP_660305.2:p.Thr491Ile
NR_026699.2:n.1562C>T
NR_026700.2:n.688-20C>T
NR_026701.2:n.1560C>T
NR_026702.2:n.618-20C>T
NM_001144951.2:c.*591C>T	NP_001138423.1:n.*591C>T