Canonical Allele Identifier: CA2844640151

Gene: UNG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109100430A>C , CM000674.2:g.109100430A>C	GRCh38
NC_000012.11:g.109538235A>C , CM000674.1:g.109538235A>C	GRCh37
NC_000012.10:g.108022618A>C	NCBI36
NG_007284.1:g.7821A>C , LRG_124:g.7821A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539287.6:c.408+1146A>C	ENSP00000440784.1:n.408+1146A>C
ENST00000699559.1:c.408+1146A>C	ENSP00000514433.1:n.408+1146A>C
ENST00000699560.1:c.313-1472A>C	ENSP00000514434.1:n.313-1472A>C
ENST00000699561.1:c.408+1146A>C	ENSP00000514435.1:n.408+1146A>C
ENST00000699562.1:c.408+1146A>C	ENSP00000514436.1:n.408+1146A>C
ENST00000699563.1:c.408+1146A>C	ENSP00000514437.1:n.408+1146A>C
ENST00000699564.1:c.408+1146A>C	ENSP00000514438.1:n.408+1146A>C
ENST00000699565.1:c.408+1146A>C	ENSP00000514439.1:n.408+1146A>C
ENST00000699566.1:c.513+1146A>C	ENSP00000514440.1:n.513+1146A>C
ENST00000699567.1:c.408+1146A>C	ENSP00000514441.1:n.408+1146A>C
ENST00000242576.7:c.435+1146A>C MANE Select	ENSP00000242576.3:n.435+1146A>C
ENST00000242576.6:c.435+1146A>C	ENSP00000242576.2:n.435+1146A>C
ENST00000336865.6:c.408+1146A>C	ENSP00000337398.2:n.408+1146A>C
ENST00000446767.2:c.408+1146A>C	ENSP00000400287.2:n.408+1146A>C
ENST00000539287.5:c.408+1146A>C	ENSP00000440784.1:n.408+1146A>C
NM_003362.3:c.408+1146A>C	NP_003353.1:n.408+1146A>C
NM_080911.2:c.435+1146A>C	NP_550433.1:n.435+1146A>C
NM_003362.4:c.408+1146A>C	NP_003353.1:n.408+1146A>C
NM_080911.3:c.435+1146A>C MANE Select	NP_550433.1:n.435+1146A>C