Canonical Allele Identifier: CA487594088

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93684958A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218612A>G , CM000676.2:g.93218612A>G	GRCh38
NC_000014.8:g.93684958A>G , CM000676.1:g.93684958A>G	GRCh37
NC_000014.7:g.92754711A>G	NCBI36
NG_051089.1:g.16557A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.687A>G MANE Select	ENSP00000013070.6:p.Gly229=
ENST00000013070.10:c.687A>G	ENSP00000013070.6:p.Gly229=
ENST00000416753.5:c.459A>G	ENSP00000391706.2:p.Gly153=
ENST00000553674.1:c.*388A>G	ENSP00000450470.1:n.*388A>G
ENST00000553857.5:c.378+3331A>G
ENST00000556871.5:c.396A>G	ENSP00000451022.1:p.Gly132=
NM_175748.3:c.687A>G	NP_786924.2:p.Gly229=
NR_038150.1:n.789A>G
NM_175748.4:c.687A>G MANE Select	NP_786924.2:p.Gly229=
NR_038150.2:n.589A>G