Canonical Allele Identifier: CA487594111
Gene: UBR7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.93684997A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218651A>G , CM000676.2:g.93218651A>G GRCh38
NC_000014.8:g.93684997A>G , CM000676.1:g.93684997A>G GRCh37
NC_000014.7:g.92754750A>G NCBI36
NG_051089.1:g.16596A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000013070.11:c.726A>G MANE Select ENSP00000013070.6:p.Glu242=
ENST00000013070.10:c.726A>G ENSP00000013070.6:p.Glu242=
ENST00000416753.5:c.498A>G ENSP00000391706.2:p.Glu166=
ENST00000553674.1:c.*427A>G ENSP00000450470.1:n.*427A>G
ENST00000553857.5:c.378+3370A>G
ENST00000556871.5:c.435A>G ENSP00000451022.1:p.Glu145=
NM_175748.3:c.726A>G NP_786924.2:p.Glu242=
NR_038150.1:n.828A>G
NM_175748.4:c.726A>G MANE Select NP_786924.2:p.Glu242=
NR_038150.2:n.628A>G
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