Canonical Allele Identifier: CA2155441022

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218556T= , CM000676.2:g.93218556T=	GRCh38
NC_000014.8:g.93684902T= , CM000676.1:g.93684902T=	GRCh37
NC_000014.7:g.92754655T=	NCBI36
NG_051089.1:g.16501T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.631T= MANE Select	ENSP00000013070.6:p.Leu211=
ENST00000013070.10:c.631T=	ENSP00000013070.6:p.Leu211=
ENST00000416753.5:c.403T=	ENSP00000391706.2:p.Leu135=
ENST00000553674.1:c.*332T=	ENSP00000450470.1:n.*332T=
ENST00000553857.5:c.378+3275T=
ENST00000554232.5:c.535T=
ENST00000556871.5:c.340T=	ENSP00000451022.1:p.Leu114=
ENST00000557048.1:n.540T=
NM_175748.3:c.631T=	NP_786924.2:p.Leu211=
NR_038150.1:n.733T=
NM_175748.4:c.631T= MANE Select	NP_786924.2:p.Leu211=
NR_038150.2:n.533T=