Canonical Allele Identifier: CA2062256445
Gene: UNG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.109100331G= , CM000674.2:g.109100331G= GRCh38
NC_000012.11:g.109538136G= , CM000674.1:g.109538136G= GRCh37
NC_000012.10:g.108022519G= NCBI36
NG_007284.1:g.7722G= , LRG_124:g.7722G=

Transcript Alleles

HGVS Amino-acid change
ENST00000539287.6:c.408+1047G= ENSP00000440784.1:n.408+1047G=
ENST00000699559.1:c.408+1047G= ENSP00000514433.1:n.408+1047G=
ENST00000699560.1:c.313-1571G= ENSP00000514434.1:n.313-1571G=
ENST00000699561.1:c.408+1047G= ENSP00000514435.1:n.408+1047G=
ENST00000699562.1:c.408+1047G= ENSP00000514436.1:n.408+1047G=
ENST00000699563.1:c.408+1047G= ENSP00000514437.1:n.408+1047G=
ENST00000699564.1:c.408+1047G= ENSP00000514438.1:n.408+1047G=
ENST00000699565.1:c.408+1047G= ENSP00000514439.1:n.408+1047G=
ENST00000699566.1:c.513+1047G= ENSP00000514440.1:n.513+1047G=
ENST00000699567.1:c.408+1047G= ENSP00000514441.1:n.408+1047G=
ENST00000242576.7:c.435+1047G= MANE Select ENSP00000242576.3:n.435+1047G=
ENST00000242576.6:c.435+1047G= ENSP00000242576.2:n.435+1047G=
ENST00000336865.6:c.408+1047G= ENSP00000337398.2:n.408+1047G=
ENST00000446767.2:c.408+1047G= ENSP00000400287.2:n.408+1047G=
ENST00000539287.5:c.408+1047G= ENSP00000440784.1:n.408+1047G=
NM_003362.3:c.408+1047G= NP_003353.1:n.408+1047G=
NM_080911.2:c.435+1047G= NP_550433.1:n.435+1047G=
NM_003362.4:c.408+1047G= NP_003353.1:n.408+1047G=
NM_080911.3:c.435+1047G= MANE Select NP_550433.1:n.435+1047G=