Canonical Allele Identifier: CA390810963
Gene: UBR7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.93684968G>C (hg19) chr14:g.93218622G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218622G>C , CM000676.2:g.93218622G>C GRCh38
NC_000014.8:g.93684968G>C , CM000676.1:g.93684968G>C GRCh37
NC_000014.7:g.92754721G>C NCBI36
NG_051089.1:g.16567G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.697G>C MANE Select ENSP00000013070.6:p.Asp233His
ENST00000013070.10:c.697G>C ENSP00000013070.6:p.Asp233His
ENST00000416753.5:c.469G>C ENSP00000391706.2:p.Asp157His
ENST00000553674.1:c.*398G>C ENSP00000450470.1:n.*398G>C
ENST00000553857.5:c.378+3341G>C
ENST00000556871.5:c.406G>C ENSP00000451022.1:p.Asp136His
NM_175748.3:c.697G>C NP_786924.2:p.Asp233His
NR_038150.1:n.799G>C
NM_175748.4:c.697G>C MANE Select NP_786924.2:p.Asp233His
NR_038150.2:n.599G>C
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