Canonical Allele Identifier: CA487594147
Gene: UBR7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.93685060T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218714T>A , CM000676.2:g.93218714T>A GRCh38
NC_000014.8:g.93685060T>A , CM000676.1:g.93685060T>A GRCh37
NC_000014.7:g.92754813T>A NCBI36
NG_051089.1:g.16659T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.789T>A MANE Select ENSP00000013070.6:p.Ser263=
ENST00000013070.10:c.789T>A ENSP00000013070.6:p.Ser263=
ENST00000416753.5:c.561T>A ENSP00000391706.2:p.Ser187=
ENST00000553674.1:c.*490T>A ENSP00000450470.1:n.*490T>A
ENST00000553857.5:c.378+3433T>A
ENST00000555329.1:c.34T>A
NM_175748.3:c.789T>A NP_786924.2:p.Ser263=
NR_038150.1:n.891T>A
NM_175748.4:c.789T>A MANE Select NP_786924.2:p.Ser263=
NR_038150.2:n.691T>A
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