Canonical Allele Identifier: CA2552876921
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218340G>T , CM000676.2:g.93218340G>T GRCh38
NC_000014.8:g.93684686G>T , CM000676.1:g.93684686G>T GRCh37
NC_000014.7:g.92754439G>T NCBI36
NG_051089.1:g.16285G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-187G>T MANE Select ENSP00000013070.6:n.602-187G>T
ENST00000013070.10:c.602-187G>T ENSP00000013070.6:n.602-187G>T
ENST00000416753.5:c.374-187G>T ENSP00000391706.2:n.374-187G>T
ENST00000553674.1:c.*303-187G>T ENSP00000450470.1:n.*303-187G>T
ENST00000553857.5:c.378+3059G>T
ENST00000554232.5:c.506-187G>T ENSP00000450645.1:n.506-187G>T
ENST00000556871.5:c.311-187G>T ENSP00000451022.1:n.311-187G>T
ENST00000557048.1:n.511-187G>T
NM_175748.3:c.602-187G>T NP_786924.2:n.602-187G>T
NR_038150.1:n.704-187G>T
NM_175748.4:c.602-187G>T MANE Select NP_786924.2:n.602-187G>T
NR_038150.2:n.504-187G>T