Canonical Allele Identifier: CA2155441007

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218511T= , CM000676.2:g.93218511T=	GRCh38
NC_000014.8:g.93684857T= , CM000676.1:g.93684857T=	GRCh37
NC_000014.7:g.92754610T=	NCBI36
NG_051089.1:g.16456T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-16T= MANE Select	ENSP00000013070.6:n.602-16T=
ENST00000013070.10:c.602-16T=	ENSP00000013070.6:n.602-16T=
ENST00000416753.5:c.374-16T=	ENSP00000391706.2:n.374-16T=
ENST00000553674.1:c.*303-16T=	ENSP00000450470.1:n.*303-16T=
ENST00000553857.5:c.378+3230T=
ENST00000554232.5:c.506-16T=	ENSP00000450645.1:n.506-16T=
ENST00000556871.5:c.311-16T=	ENSP00000451022.1:n.311-16T=
ENST00000557048.1:n.511-16T=
NM_175748.3:c.602-16T=	NP_786924.2:n.602-16T=
NR_038150.1:n.704-16T=
NM_175748.4:c.602-16T= MANE Select	NP_786924.2:n.602-16T=
NR_038150.2:n.504-16T=