Canonical Allele Identifier: CA390811557
Gene: UBR7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr14:g.93685075T>A (hg19) chr14:g.93218729T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.93218729T>A , CM000676.2:g.93218729T>A GRCh38
NC_000014.8:g.93685075T>A , CM000676.1:g.93685075T>A GRCh37
NC_000014.7:g.92754828T>A NCBI36
NG_051089.1:g.16674T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000013070.11:c.804T>A MANE Select ENSP00000013070.6:p.Asp268Glu
ENST00000013070.10:c.804T>A ENSP00000013070.6:p.Asp268Glu
ENST00000416753.5:c.576T>A ENSP00000391706.2:p.Asp192Glu
ENST00000553674.1:c.*505T>A ENSP00000450470.1:n.*505T>A
ENST00000553857.5:c.378+3448T>A
ENST00000555329.1:c.49T>A
NM_175748.3:c.804T>A NP_786924.2:p.Asp268Glu
NR_038150.1:n.906T>A
NM_175748.4:c.804T>A MANE Select NP_786924.2:p.Asp268Glu
NR_038150.2:n.706T>A
Search 100 bp 5'
Search 100 bp 3'