Canonical Allele Identifier: CA390811095

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93685004A>T (hg19) ; chr14:g.93218658A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218658A>T , CM000676.2:g.93218658A>T	GRCh38
NC_000014.8:g.93685004A>T , CM000676.1:g.93685004A>T	GRCh37
NC_000014.7:g.92754757A>T	NCBI36
NG_051089.1:g.16603A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.733A>T MANE Select	ENSP00000013070.6:p.Lys245Ter
ENST00000013070.10:c.733A>T	ENSP00000013070.6:p.Lys245Ter
ENST00000416753.5:c.505A>T	ENSP00000391706.2:p.Lys169Ter
ENST00000553674.1:c.*434A>T	ENSP00000450470.1:n.*434A>T
ENST00000553857.5:c.378+3377A>T
ENST00000556871.5:c.442A>T	ENSP00000451022.1:p.Lys148Ter
NM_175748.3:c.733A>T	NP_786924.2:p.Lys245Ter
NR_038150.1:n.835A>T
NM_175748.4:c.733A>T MANE Select	NP_786924.2:p.Lys245Ter
NR_038150.2:n.635A>T