Canonical Allele Identifier: CA487594137

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93685045A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218699A>G , CM000676.2:g.93218699A>G	GRCh38
NC_000014.8:g.93685045A>G , CM000676.1:g.93685045A>G	GRCh37
NC_000014.7:g.92754798A>G	NCBI36
NG_051089.1:g.16644A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.774A>G MANE Select	ENSP00000013070.6:p.Glu258=
ENST00000013070.10:c.774A>G	ENSP00000013070.6:p.Glu258=
ENST00000416753.5:c.546A>G	ENSP00000391706.2:p.Glu182=
ENST00000553674.1:c.*475A>G	ENSP00000450470.1:n.*475A>G
ENST00000553857.5:c.378+3418A>G
ENST00000555329.1:c.19A>G
NM_175748.3:c.774A>G	NP_786924.2:p.Glu258=
NR_038150.1:n.876A>G
NM_175748.4:c.774A>G MANE Select	NP_786924.2:p.Glu258=
NR_038150.2:n.676A>G