Canonical Allele Identifier: CA2155441013

Gene: UBR7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218538T= , CM000676.2:g.93218538T=	GRCh38
NC_000014.8:g.93684884T= , CM000676.1:g.93684884T=	GRCh37
NC_000014.7:g.92754637T=	NCBI36
NG_051089.1:g.16483T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.613T= MANE Select	ENSP00000013070.6:p.Ser205=
ENST00000013070.10:c.613T=	ENSP00000013070.6:p.Ser205=
ENST00000416753.5:c.385T=	ENSP00000391706.2:p.Ser129=
ENST00000553674.1:c.*314T=	ENSP00000450470.1:n.*314T=
ENST00000553857.5:c.378+3257T=
ENST00000554232.5:c.517T=	ENSP00000450645.1:p.Ser173=
ENST00000556871.5:c.322T=	ENSP00000451022.1:p.Ser108=
ENST00000557048.1:n.522T=
NM_175748.3:c.613T=	NP_786924.2:p.Ser205=
NR_038150.1:n.715T=
NM_175748.4:c.613T= MANE Select	NP_786924.2:p.Ser205=
NR_038150.2:n.515T=