Canonical Allele Identifier: CA433752084

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293147-G-T
• MyVariant Identifiers: chr3:g.52327163G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293147G>T , CM000665.2:g.52293147G>T	GRCh38
NC_000003.11:g.52327163G>T , CM000665.1:g.52327163G>T	GRCh37
NC_000003.10:g.52302203G>T	NCBI36
NG_023246.1:g.10328G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*21G>T MANE Select	ENSP00000389175.2:n.*21G>T
ENST00000436784.6:c.*21G>T	ENSP00000389175.2:n.*21G>T
ENST00000461183.5:c.*13G>T	ENSP00000417264.1:n.*13G>T
ENST00000471180.5:c.*13G>T	ENSP00000417526.1:n.*13G>T
ENST00000473032.5:c.*13G>T	ENSP00000418951.1:n.*13G>T
ENST00000486393.5:c.*956G>T	ENSP00000419868.1:n.*956G>T
ENST00000489173.1:n.1887G>T
NM_145262.3:c.*21G>T	NP_660305.2:n.*21G>T
NR_026699.1:n.1691G>T
NR_026700.1:n.797G>T
NR_026701.1:n.1689G>T
NR_026702.1:n.727G>T
XM_005264878.2:c.*712G>T	XP_005264935.1:n.*712G>T
XR_245095.2:n.2844G>T
XM_017005730.1:c.*21G>T	XP_016861219.1:n.*21G>T
XM_024453351.1:c.*21G>T	XP_024309119.1:n.*21G>T
XM_024453352.1:c.*712G>T	XP_024309120.1:n.*712G>T
XR_001740022.2:n.3495G>T
XR_001740023.2:n.3019G>T
XR_245095.4:n.2845G>T
NM_145262.4:c.*21G>T MANE Select	NP_660305.2:n.*21G>T
NR_026699.2:n.1683G>T
NR_026700.2:n.789G>T
NR_026701.2:n.1681G>T
NR_026702.2:n.719G>T
NM_001144951.2:c.*712G>T	NP_001138423.1:n.*712G>T