Canonical Allele Identifier: CA243395986

Gene: UNG

Linked Data

• dbSNP Id: rs889273631
• MyVariant Identifiers: chr12:g.109538293C>G (hg19) ; chr12:g.109100488C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109100488C>G , CM000674.2:g.109100488C>G	GRCh38
NC_000012.11:g.109538293C>G , CM000674.1:g.109538293C>G	GRCh37
NC_000012.10:g.108022676C>G	NCBI36
NG_007284.1:g.7879C>G , LRG_124:g.7879C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000539287.6:c.408+1204C>G	ENSP00000440784.1:n.408+1204C>G
ENST00000699559.1:c.408+1204C>G	ENSP00000514433.1:n.408+1204C>G
ENST00000699560.1:c.313-1414C>G	ENSP00000514434.1:n.313-1414C>G
ENST00000699561.1:c.408+1204C>G	ENSP00000514435.1:n.408+1204C>G
ENST00000699562.1:c.408+1204C>G	ENSP00000514436.1:n.408+1204C>G
ENST00000699563.1:c.408+1204C>G	ENSP00000514437.1:n.408+1204C>G
ENST00000699564.1:c.408+1204C>G	ENSP00000514438.1:n.408+1204C>G
ENST00000699565.1:c.408+1204C>G	ENSP00000514439.1:n.408+1204C>G
ENST00000699566.1:c.513+1204C>G	ENSP00000514440.1:n.513+1204C>G
ENST00000699567.1:c.408+1204C>G	ENSP00000514441.1:n.408+1204C>G
ENST00000242576.7:c.435+1204C>G MANE Select	ENSP00000242576.3:n.435+1204C>G
ENST00000242576.6:c.435+1204C>G	ENSP00000242576.2:n.435+1204C>G
ENST00000336865.6:c.408+1204C>G	ENSP00000337398.2:n.408+1204C>G
ENST00000446767.2:c.408+1204C>G	ENSP00000400287.2:n.408+1204C>G
ENST00000539287.5:c.408+1204C>G	ENSP00000440784.1:n.408+1204C>G
NM_003362.3:c.408+1204C>G	NP_003353.1:n.408+1204C>G
NM_080911.2:c.435+1204C>G	NP_550433.1:n.435+1204C>G
NM_003362.4:c.408+1204C>G	NP_003353.1:n.408+1204C>G
NM_080911.3:c.435+1204C>G MANE Select	NP_550433.1:n.435+1204C>G