Canonical Allele Identifier: CA487594036

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93684874A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218528A>T , CM000676.2:g.93218528A>T	GRCh38
NC_000014.8:g.93684874A>T , CM000676.1:g.93684874A>T	GRCh37
NC_000014.7:g.92754627A>T	NCBI36
NG_051089.1:g.16473A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.603A>T MANE Select	ENSP00000013070.6:p.Val201=
ENST00000013070.10:c.603A>T	ENSP00000013070.6:p.Val201=
ENST00000416753.5:c.375A>T	ENSP00000391706.2:p.Val125=
ENST00000553674.1:c.*304A>T	ENSP00000450470.1:n.*304A>T
ENST00000553857.5:c.378+3247A>T
ENST00000554232.5:c.507A>T	ENSP00000450645.1:p.Val169=
ENST00000556871.5:c.312A>T	ENSP00000451022.1:p.Val104=
ENST00000557048.1:n.512A>T
NM_175748.3:c.603A>T	NP_786924.2:p.Val201=
NR_038150.1:n.705A>T
NM_175748.4:c.603A>T MANE Select	NP_786924.2:p.Val201=
NR_038150.2:n.505A>T