Canonical Allele Identifier: CA10640037

Gene: UNG

Linked Data

• ClinVar Variation Id: 306990
• ClinVar RCV Id: RCV000309188
• dbSNP Id: rs775022596
• gnomAD v3: 12-109110624-A-C
• gnomAD v4: 12-109110624-A-C
• MyVariant Identifiers: chr12:g.109548429A>C (hg19) ; chr12:g.109110624A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109110624A>C , CM000674.2:g.109110624A>C	GRCh38
NC_000012.11:g.109548429A>C , CM000674.1:g.109548429A>C	GRCh37
NC_000012.10:g.108032812A>C	NCBI36
NG_007284.1:g.18015A>C , LRG_124:g.18015A>C
NG_046907.1:g.4441A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000539287.6:c.*913A>C	ENSP00000440784.1:n.*913A>C
ENST00000699559.1:c.*868A>C	ENSP00000514433.1:n.*868A>C
ENST00000699560.1:c.*655A>C	ENSP00000514434.1:n.*655A>C
ENST00000699562.1:c.*655A>C	ENSP00000514436.1:n.*655A>C
ENST00000699563.1:c.774+7013A>C	ENSP00000514437.1:n.774+7013A>C
ENST00000699565.1:c.1587A>C	ENSP00000514439.1:n.1587A>C
ENST00000699566.1:c.1675A>C	ENSP00000514440.1:n.1675A>C
ENST00000699567.1:c.1481A>C	ENSP00000514441.1:n.1481A>C
ENST00000242576.7:c.*655A>C MANE Select	ENSP00000242576.3:n.*655A>C
ENST00000242576.6:c.*655A>C	ENSP00000242576.2:n.*655A>C
ENST00000336865.6:c.*655A>C	ENSP00000337398.2:n.*655A>C
ENST00000446767.2:c.*1046A>C	ENSP00000400287.2:n.*1046A>C
ENST00000539287.5:c.*910A>C	ENSP00000440784.1:n.*910A>C
NM_003362.3:c.*655A>C	NP_003353.1:n.*655A>C
NM_080911.2:c.*655A>C	NP_550433.1:n.*655A>C
NM_003362.4:c.*655A>C	NP_003353.1:n.*655A>C
NM_080911.3:c.*655A>C MANE Select	NP_550433.1:n.*655A>C