Canonical Allele Identifier: CA390810664

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93684879A>C (hg19) ; chr14:g.93218533A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218533A>C , CM000676.2:g.93218533A>C	GRCh38
NC_000014.8:g.93684879A>C , CM000676.1:g.93684879A>C	GRCh37
NC_000014.7:g.92754632A>C	NCBI36
NG_051089.1:g.16478A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.608A>C MANE Select	ENSP00000013070.6:p.Lys203Thr
ENST00000013070.10:c.608A>C	ENSP00000013070.6:p.Lys203Thr
ENST00000416753.5:c.380A>C	ENSP00000391706.2:p.Lys127Thr
ENST00000553674.1:c.*309A>C	ENSP00000450470.1:n.*309A>C
ENST00000553857.5:c.378+3252A>C
ENST00000554232.5:c.512A>C	ENSP00000450645.1:p.Lys171Thr
ENST00000556871.5:c.317A>C	ENSP00000451022.1:p.Lys106Thr
ENST00000557048.1:n.517A>C
NM_175748.3:c.608A>C	NP_786924.2:p.Lys203Thr
NR_038150.1:n.710A>C
NM_175748.4:c.608A>C MANE Select	NP_786924.2:p.Lys203Thr
NR_038150.2:n.510A>C