Canonical Allele Identifier: CA487594044

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93684886C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218540C>G , CM000676.2:g.93218540C>G	GRCh38
NC_000014.8:g.93684886C>G , CM000676.1:g.93684886C>G	GRCh37
NC_000014.7:g.92754639C>G	NCBI36
NG_051089.1:g.16485C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.615C>G MANE Select	ENSP00000013070.6:p.Ser205=
ENST00000013070.10:c.615C>G	ENSP00000013070.6:p.Ser205=
ENST00000416753.5:c.387C>G	ENSP00000391706.2:p.Ser129=
ENST00000553674.1:c.*316C>G	ENSP00000450470.1:n.*316C>G
ENST00000553857.5:c.378+3259C>G
ENST00000554232.5:c.519C>G	ENSP00000450645.1:p.Ser173=
ENST00000556871.5:c.324C>G	ENSP00000451022.1:p.Ser108=
ENST00000557048.1:n.524C>G
NM_175748.3:c.615C>G	NP_786924.2:p.Ser205=
NR_038150.1:n.717C>G
NM_175748.4:c.615C>G MANE Select	NP_786924.2:p.Ser205=
NR_038150.2:n.517C>G