Canonical Allele Identifier: CA2575610201
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218477A>T , CM000676.2:g.93218477A>T GRCh38
NC_000014.8:g.93684823A>T , CM000676.1:g.93684823A>T GRCh37
NC_000014.7:g.92754576A>T NCBI36
NG_051089.1:g.16422A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-50A>T MANE Select ENSP00000013070.6:n.602-50A>T
ENST00000013070.10:c.602-50A>T ENSP00000013070.6:n.602-50A>T
ENST00000416753.5:c.374-50A>T ENSP00000391706.2:n.374-50A>T
ENST00000553674.1:c.*303-50A>T ENSP00000450470.1:n.*303-50A>T
ENST00000553857.5:c.378+3196A>T
ENST00000554232.5:c.506-50A>T ENSP00000450645.1:n.506-50A>T
ENST00000556871.5:c.311-50A>T ENSP00000451022.1:n.311-50A>T
ENST00000557048.1:n.511-50A>T
NM_175748.3:c.602-50A>T NP_786924.2:n.602-50A>T
NR_038150.1:n.704-50A>T
NM_175748.4:c.602-50A>T MANE Select NP_786924.2:n.602-50A>T
NR_038150.2:n.504-50A>T