Canonical Allele Identifier: CA122119

Gene: UNG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.109103562T>C , CM000674.2:g.109103562T>C	GRCh38
NC_000012.11:g.109541367T>C , CM000674.1:g.109541367T>C	GRCh37
NC_000012.10:g.108025750T>C	NCBI36
NG_007284.1:g.10953T>C , LRG_124:g.10953T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_080911.3:c.752T>C MANE Select	NP_550433.1:p.Phe251Ser
ENST00000242576.7:c.752T>C MANE Select	ENSP00000242576.3:p.Phe251Ser
NM_003362.3:c.725T>C	NP_003353.1:p.Phe242Ser
NM_003362.4:c.725T>C	NP_003353.1:p.Phe242Ser
NM_080911.2:c.752T>C	NP_550433.1:p.Phe251Ser
ENST00000242576.6:c.752T>C	ENSP00000242576.2:p.Phe251Ser
ENST00000336865.6:c.725T>C	ENSP00000337398.2:p.Phe242Ser
ENST00000446767.2:c.*201T>C	ENSP00000400287.2:n.*201T>C
ENST00000539287.5:c.725T>C	ENSP00000440784.1:p.Phe242Ser
ENST00000539287.6:c.725T>C	ENSP00000440784.1:p.Phe242Ser
ENST00000699559.1:c.725T>C	ENSP00000514433.1:p.Phe242Ser
ENST00000699560.1:c.629T>C	ENSP00000514434.1:p.Phe210Ser
ENST00000699561.1:c.725T>C	ENSP00000514435.1:p.Phe242Ser
ENST00000699562.1:c.725T>C	ENSP00000514436.1:p.Phe242Ser
ENST00000699563.1:c.725T>C	ENSP00000514437.1:p.Phe242Ser
ENST00000699564.1:c.*181T>C	ENSP00000514438.1:n.*181T>C
ENST00000699565.1:c.742T>C	ENSP00000514439.1:n.742T>C
ENST00000699566.1:c.830T>C	ENSP00000514440.1:n.830T>C
ENST00000699567.1:c.636T>C	ENSP00000514441.1:n.636T>C