Canonical Allele Identifier: CA2062259379

Gene: UNG

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539287.6:c.725T=	ENSP00000440784.1:p.Phe242=
ENST00000699559.1:c.725T=	ENSP00000514433.1:p.Phe242=
ENST00000699560.1:c.629T=	ENSP00000514434.1:p.Phe210=
ENST00000699561.1:c.725T=	ENSP00000514435.1:p.Phe242=
ENST00000699562.1:c.725T=	ENSP00000514436.1:p.Phe242=
ENST00000699563.1:c.725T=	ENSP00000514437.1:p.Phe242=
ENST00000699564.1:c.*181T=	ENSP00000514438.1:n.*181T=
ENST00000699565.1:c.742T=	ENSP00000514439.1:n.742T=
ENST00000699566.1:c.830T=	ENSP00000514440.1:n.830T=
ENST00000699567.1:c.636T=	ENSP00000514441.1:n.636T=
ENST00000242576.7:c.752T= MANE Select	ENSP00000242576.3:p.Phe251=
ENST00000242576.6:c.752T=	ENSP00000242576.2:p.Phe251=
ENST00000336865.6:c.725T=	ENSP00000337398.2:p.Phe242=
ENST00000446767.2:c.*201T=	ENSP00000400287.2:n.*201T=
ENST00000539287.5:c.725T=	ENSP00000440784.1:p.Phe242=
NM_003362.3:c.725T=	NP_003353.1:p.Phe242=
NM_080911.2:c.752T=	NP_550433.1:p.Phe251=
NM_003362.4:c.725T=	NP_003353.1:p.Phe242=
NM_080911.3:c.752T= MANE Select	NP_550433.1:p.Phe251=