Canonical Allele Identifier: CA543056384

Gene: GLYCTK

Linked Data

• dbSNP Id: rs1242422230
• gnomAD v2: 3-52327178-C-G
• gnomAD v3: 3-52293162-C-G
• gnomAD v4: 3-52293162-C-G
• MyVariant Identifiers: chr3:g.52327178C>G (hg19) ; chr3:g.52293162C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.52293162C>G , CM000665.2:g.52293162C>G	GRCh38
NC_000003.11:g.52327178C>G , CM000665.1:g.52327178C>G	GRCh37
NC_000003.10:g.52302218C>G	NCBI36
NG_023246.1:g.10343C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436784.7:c.*36C>G MANE Select	ENSP00000389175.2:n.*36C>G
ENST00000436784.6:c.*36C>G	ENSP00000389175.2:n.*36C>G
ENST00000461183.5:c.*28C>G	ENSP00000417264.1:n.*28C>G
ENST00000471180.5:c.*28C>G	ENSP00000417526.1:n.*28C>G
ENST00000473032.5:c.*28C>G	ENSP00000418951.1:n.*28C>G
ENST00000486393.5:c.*971C>G	ENSP00000419868.1:n.*971C>G
ENST00000489173.1:n.1902C>G
NM_145262.3:c.*36C>G	NP_660305.2:n.*36C>G
NR_026699.1:n.1706C>G
NR_026700.1:n.812C>G
NR_026701.1:n.1704C>G
NR_026702.1:n.742C>G
XM_005264878.2:c.*727C>G	XP_005264935.1:n.*727C>G
XR_245095.2:n.2859C>G
XM_017005730.1:c.*36C>G	XP_016861219.1:n.*36C>G
XM_024453351.1:c.*36C>G	XP_024309119.1:n.*36C>G
XM_024453352.1:c.*727C>G	XP_024309120.1:n.*727C>G
XR_001740022.2:n.3510C>G
XR_001740023.2:n.3034C>G
XR_245095.4:n.2860C>G
NM_145262.4:c.*36C>G MANE Select	NP_660305.2:n.*36C>G
NR_026699.2:n.1698C>G
NR_026700.2:n.804C>G
NR_026701.2:n.1696C>G
NR_026702.2:n.734C>G
NM_001144951.2:c.*727C>G	NP_001138423.1:n.*727C>G