Canonical Allele Identifier: CA390811465

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93685067G>T (hg19) ; chr14:g.93218721G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218721G>T , CM000676.2:g.93218721G>T	GRCh38
NC_000014.8:g.93685067G>T , CM000676.1:g.93685067G>T	GRCh37
NC_000014.7:g.92754820G>T	NCBI36
NG_051089.1:g.16666G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.796G>T MANE Select	ENSP00000013070.6:p.Glu266Ter
ENST00000013070.10:c.796G>T	ENSP00000013070.6:p.Glu266Ter
ENST00000416753.5:c.568G>T	ENSP00000391706.2:p.Glu190Ter
ENST00000553674.1:c.*497G>T	ENSP00000450470.1:n.*497G>T
ENST00000553857.5:c.378+3440G>T
ENST00000555329.1:c.41G>T
NM_175748.3:c.796G>T	NP_786924.2:p.Glu266Ter
NR_038150.1:n.898G>T
NM_175748.4:c.796G>T MANE Select	NP_786924.2:p.Glu266Ter
NR_038150.2:n.698G>T