Canonical Allele Identifier: CA2155441018

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218546G= , CM000676.2:g.93218546G=	GRCh38
NC_000014.8:g.93684892G= , CM000676.1:g.93684892G=	GRCh37
NC_000014.7:g.92754645G=	NCBI36
NG_051089.1:g.16491G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.621G= MANE Select	ENSP00000013070.6:p.Glu207=
ENST00000013070.10:c.621G=	ENSP00000013070.6:p.Glu207=
ENST00000416753.5:c.393G=	ENSP00000391706.2:p.Glu131=
ENST00000553674.1:c.*322G=	ENSP00000450470.1:n.*322G=
ENST00000553857.5:c.378+3265G=
ENST00000554232.5:c.525G=	ENSP00000450645.1:p.Glu175=
ENST00000556871.5:c.330G=	ENSP00000451022.1:p.Glu110=
ENST00000557048.1:n.530G=
NM_175748.3:c.621G=	NP_786924.2:p.Glu207=
NR_038150.1:n.723G=
NM_175748.4:c.621G= MANE Select	NP_786924.2:p.Glu207=
NR_038150.2:n.523G=