Canonical Allele Identifier: CA2802634112
Gene: UBR7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218365C>G , CM000676.2:g.93218365C>G GRCh38
NC_000014.8:g.93684711C>G , CM000676.1:g.93684711C>G GRCh37
NC_000014.7:g.92754464C>G NCBI36
NG_051089.1:g.16310C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.602-162C>G MANE Select ENSP00000013070.6:n.602-162C>G
ENST00000013070.10:c.602-162C>G ENSP00000013070.6:n.602-162C>G
ENST00000416753.5:c.374-162C>G ENSP00000391706.2:n.374-162C>G
ENST00000553674.1:c.*303-162C>G ENSP00000450470.1:n.*303-162C>G
ENST00000553857.5:c.378+3084C>G
ENST00000554232.5:c.506-162C>G ENSP00000450645.1:n.506-162C>G
ENST00000556871.5:c.311-162C>G ENSP00000451022.1:n.311-162C>G
ENST00000557048.1:n.511-162C>G
NM_175748.3:c.602-162C>G NP_786924.2:n.602-162C>G
NR_038150.1:n.704-162C>G
NM_175748.4:c.602-162C>G MANE Select NP_786924.2:n.602-162C>G
NR_038150.2:n.504-162C>G