Canonical Allele Identifier: CA390810881
Gene: UBR7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.93684947C>A (hg19) chr14:g.93218601C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218601C>A , CM000676.2:g.93218601C>A GRCh38
NC_000014.8:g.93684947C>A , CM000676.1:g.93684947C>A GRCh37
NC_000014.7:g.92754700C>A NCBI36
NG_051089.1:g.16546C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.676C>A MANE Select ENSP00000013070.6:p.Pro226Thr
ENST00000013070.10:c.676C>A ENSP00000013070.6:p.Pro226Thr
ENST00000416753.5:c.448C>A ENSP00000391706.2:p.Pro150Thr
ENST00000553674.1:c.*377C>A ENSP00000450470.1:n.*377C>A
ENST00000553857.5:c.378+3320C>A
ENST00000556871.5:c.385C>A ENSP00000451022.1:p.Pro129Thr
NM_175748.3:c.676C>A NP_786924.2:p.Pro226Thr
NR_038150.1:n.778C>A
NM_175748.4:c.676C>A MANE Select NP_786924.2:p.Pro226Thr
NR_038150.2:n.578C>A
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