Canonical Allele Identifier: CA2155441008

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218522C= , CM000676.2:g.93218522C=	GRCh38
NC_000014.8:g.93684868C= , CM000676.1:g.93684868C=	GRCh37
NC_000014.7:g.92754621C=	NCBI36
NG_051089.1:g.16467C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-5C= MANE Select	ENSP00000013070.6:n.602-5C=
ENST00000013070.10:c.602-5C=	ENSP00000013070.6:n.602-5C=
ENST00000416753.5:c.374-5C=	ENSP00000391706.2:n.374-5C=
ENST00000553674.1:c.*303-5C=	ENSP00000450470.1:n.*303-5C=
ENST00000553857.5:c.378+3241C=
ENST00000554232.5:c.506-5C=	ENSP00000450645.1:n.506-5C=
ENST00000556871.5:c.311-5C=	ENSP00000451022.1:n.311-5C=
ENST00000557048.1:n.511-5C=
NM_175748.3:c.602-5C=	NP_786924.2:n.602-5C=
NR_038150.1:n.704-5C=
NM_175748.4:c.602-5C= MANE Select	NP_786924.2:n.602-5C=
NR_038150.2:n.504-5C=