Canonical Allele Identifier: CA2155440966

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218427T= , CM000676.2:g.93218427T=	GRCh38
NC_000014.8:g.93684773T= , CM000676.1:g.93684773T=	GRCh37
NC_000014.7:g.92754526T=	NCBI36
NG_051089.1:g.16372T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-100T= MANE Select	ENSP00000013070.6:n.602-100T=
ENST00000013070.10:c.602-100T=	ENSP00000013070.6:n.602-100T=
ENST00000416753.5:c.374-100T=	ENSP00000391706.2:n.374-100T=
ENST00000553674.1:c.*303-100T=	ENSP00000450470.1:n.*303-100T=
ENST00000553857.5:c.378+3146T=
ENST00000554232.5:c.506-100T=	ENSP00000450645.1:n.506-100T=
ENST00000556871.5:c.311-100T=	ENSP00000451022.1:n.311-100T=
ENST00000557048.1:n.511-100T=
NM_175748.3:c.602-100T=	NP_786924.2:n.602-100T=
NR_038150.1:n.704-100T=
NM_175748.4:c.602-100T= MANE Select	NP_786924.2:n.602-100T=
NR_038150.2:n.504-100T=