Canonical Allele Identifier: CA390810662

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93684878A>G (hg19) ; chr14:g.93218532A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218532A>G , CM000676.2:g.93218532A>G	GRCh38
NC_000014.8:g.93684878A>G , CM000676.1:g.93684878A>G	GRCh37
NC_000014.7:g.92754631A>G	NCBI36
NG_051089.1:g.16477A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.607A>G MANE Select	ENSP00000013070.6:p.Lys203Glu
ENST00000013070.10:c.607A>G	ENSP00000013070.6:p.Lys203Glu
ENST00000416753.5:c.379A>G	ENSP00000391706.2:p.Lys127Glu
ENST00000553674.1:c.*308A>G	ENSP00000450470.1:n.*308A>G
ENST00000553857.5:c.378+3251A>G
ENST00000554232.5:c.511A>G	ENSP00000450645.1:p.Lys171Glu
ENST00000556871.5:c.316A>G	ENSP00000451022.1:p.Lys106Glu
ENST00000557048.1:n.516A>G
NM_175748.3:c.607A>G	NP_786924.2:p.Lys203Glu
NR_038150.1:n.709A>G
NM_175748.4:c.607A>G MANE Select	NP_786924.2:p.Lys203Glu
NR_038150.2:n.509A>G