Canonical Allele Identifier: CA2802634115
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218384G>C , CM000676.2:g.93218384G>C GRCh38
NC_000014.8:g.93684730G>C , CM000676.1:g.93684730G>C GRCh37
NC_000014.7:g.92754483G>C NCBI36
NG_051089.1:g.16329G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-143G>C MANE Select ENSP00000013070.6:n.602-143G>C
ENST00000013070.10:c.602-143G>C ENSP00000013070.6:n.602-143G>C
ENST00000416753.5:c.374-143G>C ENSP00000391706.2:n.374-143G>C
ENST00000553674.1:c.*303-143G>C ENSP00000450470.1:n.*303-143G>C
ENST00000553857.5:c.378+3103G>C
ENST00000554232.5:c.506-143G>C ENSP00000450645.1:n.506-143G>C
ENST00000556871.5:c.311-143G>C ENSP00000451022.1:n.311-143G>C
ENST00000557048.1:n.511-143G>C
NM_175748.3:c.602-143G>C NP_786924.2:n.602-143G>C
NR_038150.1:n.704-143G>C
NM_175748.4:c.602-143G>C MANE Select NP_786924.2:n.602-143G>C
NR_038150.2:n.504-143G>C