Canonical Allele Identifier: CA487594051

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93684901A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218555A>C , CM000676.2:g.93218555A>C	GRCh38
NC_000014.8:g.93684901A>C , CM000676.1:g.93684901A>C	GRCh37
NC_000014.7:g.92754654A>C	NCBI36
NG_051089.1:g.16500A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.630A>C MANE Select	ENSP00000013070.6:p.Gly210=
ENST00000013070.10:c.630A>C	ENSP00000013070.6:p.Gly210=
ENST00000416753.5:c.402A>C	ENSP00000391706.2:p.Gly134=
ENST00000553674.1:c.*331A>C	ENSP00000450470.1:n.*331A>C
ENST00000553857.5:c.378+3274A>C
ENST00000554232.5:c.534A>C	ENSP00000450645.1:p.Gly178=
ENST00000556871.5:c.339A>C	ENSP00000451022.1:p.Gly113=
ENST00000557048.1:n.539A>C
NM_175748.3:c.630A>C	NP_786924.2:p.Gly210=
NR_038150.1:n.732A>C
NM_175748.4:c.630A>C MANE Select	NP_786924.2:p.Gly210=
NR_038150.2:n.532A>C