Canonical Allele Identifier: CA353076344

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293007-G-T
• MyVariant Identifiers: chr3:g.52327023G>T (hg19) ; chr3:g.52293007G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293007G>T , CM000665.2:g.52293007G>T	GRCh38
NC_000003.11:g.52327023G>T , CM000665.1:g.52327023G>T	GRCh37
NC_000003.10:g.52302063G>T	NCBI36
NG_023246.1:g.10188G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000436784.7:c.1453G>T MANE Select	ENSP00000389175.2:p.Ala485Ser
ENST00000436784.6:c.1453G>T	ENSP00000389175.2:p.Ala485Ser
ENST00000461183.5:c.764-39G>T	ENSP00000417264.1:n.764-39G>T
ENST00000471180.5:c.635-39G>T	ENSP00000417526.1:n.635-39G>T
ENST00000473032.5:c.530-39G>T	ENSP00000418951.1:n.530-39G>T
ENST00000486393.5:c.*816G>T	ENSP00000419868.1:n.*816G>T
ENST00000489173.1:n.1747G>T
NM_145262.3:c.1453G>T	NP_660305.2:p.Ala485Ser
NR_026699.1:n.1551G>T
NR_026700.1:n.696-39G>T
NR_026701.1:n.1549G>T
NR_026702.1:n.626-39G>T
XM_005264878.2:c.*572G>T	XP_005264935.1:n.*572G>T
XR_245095.2:n.2743-39G>T
XM_017005730.1:c.1072G>T	XP_016861219.1:p.Ala358Ser
XM_024453351.1:c.1453G>T	XP_024309119.1:p.Ala485Ser
XM_024453352.1:c.*572G>T	XP_024309120.1:n.*572G>T
XR_001740022.2:n.3355G>T
XR_001740023.2:n.2918-39G>T
XR_245095.4:n.2744-39G>T
NM_145262.4:c.1453G>T MANE Select	NP_660305.2:p.Ala485Ser
NR_026699.2:n.1543G>T
NR_026700.2:n.688-39G>T
NR_026701.2:n.1541G>T
NR_026702.2:n.618-39G>T
NM_001144951.2:c.*572G>T	NP_001138423.1:n.*572G>T