Canonical Allele Identifier: CA390810669

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93684881A>C (hg19) ; chr14:g.93218535A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218535A>C , CM000676.2:g.93218535A>C	GRCh38
NC_000014.8:g.93684881A>C , CM000676.1:g.93684881A>C	GRCh37
NC_000014.7:g.92754634A>C	NCBI36
NG_051089.1:g.16480A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.610A>C MANE Select	ENSP00000013070.6:p.Ile204Leu
ENST00000013070.10:c.610A>C	ENSP00000013070.6:p.Ile204Leu
ENST00000416753.5:c.382A>C	ENSP00000391706.2:p.Ile128Leu
ENST00000553674.1:c.*311A>C	ENSP00000450470.1:n.*311A>C
ENST00000553857.5:c.378+3254A>C
ENST00000554232.5:c.514A>C	ENSP00000450645.1:p.Ile172Leu
ENST00000556871.5:c.319A>C	ENSP00000451022.1:p.Ile107Leu
ENST00000557048.1:n.519A>C
NM_175748.3:c.610A>C	NP_786924.2:p.Ile204Leu
NR_038150.1:n.712A>C
NM_175748.4:c.610A>C MANE Select	NP_786924.2:p.Ile204Leu
NR_038150.2:n.512A>C