Canonical Allele Identifier: CA390811191
Gene: UBR7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.93685026A>G (hg19) chr14:g.93218680A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218680A>G , CM000676.2:g.93218680A>G GRCh38
NC_000014.8:g.93685026A>G , CM000676.1:g.93685026A>G GRCh37
NC_000014.7:g.92754779A>G NCBI36
NG_051089.1:g.16625A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.755A>G MANE Select ENSP00000013070.6:p.Lys252Arg
ENST00000013070.10:c.755A>G ENSP00000013070.6:p.Lys252Arg
ENST00000416753.5:c.527A>G ENSP00000391706.2:p.Lys176Arg
ENST00000553674.1:c.*456A>G ENSP00000450470.1:n.*456A>G
ENST00000553857.5:c.378+3399A>G
NM_175748.3:c.755A>G NP_786924.2:p.Lys252Arg
NR_038150.1:n.857A>G
NM_175748.4:c.755A>G MANE Select NP_786924.2:p.Lys252Arg
NR_038150.2:n.657A>G
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