Canonical Allele Identifier: CA908119878

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1307119642
• gnomAD v3: 3-52293304-C-A
• gnomAD v4: 3-52293304-C-A
• MyVariant Identifiers: chr3:g.52327320C>A (hg19) ; chr3:g.52293304C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293304C>A , CM000665.2:g.52293304C>A	GRCh38
NC_000003.11:g.52327320C>A , CM000665.1:g.52327320C>A	GRCh37
NC_000003.10:g.52302360C>A	NCBI36
NG_023246.1:g.10485C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*178C>A MANE Select	ENSP00000389175.2:n.*178C>A
ENST00000436784.6:c.*178C>A	ENSP00000389175.2:n.*178C>A
ENST00000471180.5:c.*59-3C>A	ENSP00000417526.1:n.*59-3C>A
ENST00000473032.5:c.*59-3C>A	ENSP00000418951.1:n.*59-3C>A
ENST00000486393.5:c.*1113C>A	ENSP00000419868.1:n.*1113C>A
ENST00000489173.1:n.1915-3C>A
NM_145262.3:c.*178C>A	NP_660305.2:n.*178C>A
NR_026699.1:n.1848C>A
NR_026700.1:n.843-3C>A
NR_026701.1:n.1735-3C>A
NR_026702.1:n.773-3C>A
XM_005264878.2:c.*869C>A	XP_005264935.1:n.*869C>A
XR_245095.2:n.2890-3C>A
XM_017005730.1:c.*178C>A	XP_016861219.1:n.*178C>A
XM_024453351.1:c.*178C>A	XP_024309119.1:n.*178C>A
XM_024453352.1:c.*869C>A	XP_024309120.1:n.*869C>A
XR_001740022.2:n.3541-3C>A
XR_001740023.2:n.3065-3C>A
XR_245095.4:n.2891-3C>A
NM_145262.4:c.*178C>A MANE Select	NP_660305.2:n.*178C>A
NR_026699.2:n.1840C>A
NR_026700.2:n.835-3C>A
NR_026701.2:n.1727-3C>A
NR_026702.2:n.765-3C>A
NM_001144951.2:c.*869C>A	NP_001138423.1:n.*869C>A