Canonical Allele Identifier: CA433752119

Gene: GLYCTK

Linked Data

• gnomAD v4: 3-52293160-G-A
• MyVariant Identifiers: chr3:g.52327176G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293160G>A , CM000665.2:g.52293160G>A	GRCh38
NC_000003.11:g.52327176G>A , CM000665.1:g.52327176G>A	GRCh37
NC_000003.10:g.52302216G>A	NCBI36
NG_023246.1:g.10341G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*34G>A MANE Select	ENSP00000389175.2:n.*34G>A
ENST00000436784.6:c.*34G>A	ENSP00000389175.2:n.*34G>A
ENST00000461183.5:c.*26G>A	ENSP00000417264.1:n.*26G>A
ENST00000471180.5:c.*26G>A	ENSP00000417526.1:n.*26G>A
ENST00000473032.5:c.*26G>A	ENSP00000418951.1:n.*26G>A
ENST00000486393.5:c.*969G>A	ENSP00000419868.1:n.*969G>A
ENST00000489173.1:n.1900G>A
NM_145262.3:c.*34G>A	NP_660305.2:n.*34G>A
NR_026699.1:n.1704G>A
NR_026700.1:n.810G>A
NR_026701.1:n.1702G>A
NR_026702.1:n.740G>A
XM_005264878.2:c.*725G>A	XP_005264935.1:n.*725G>A
XR_245095.2:n.2857G>A
XM_017005730.1:c.*34G>A	XP_016861219.1:n.*34G>A
XM_024453351.1:c.*34G>A	XP_024309119.1:n.*34G>A
XM_024453352.1:c.*725G>A	XP_024309120.1:n.*725G>A
XR_001740022.2:n.3508G>A
XR_001740023.2:n.3032G>A
XR_245095.4:n.2858G>A
NM_145262.4:c.*34G>A MANE Select	NP_660305.2:n.*34G>A
NR_026699.2:n.1696G>A
NR_026700.2:n.802G>A
NR_026701.2:n.1694G>A
NR_026702.2:n.732G>A
NM_001144951.2:c.*725G>A	NP_001138423.1:n.*725G>A