Canonical Allele Identifier: CA390810657

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93684875A>T (hg19) ; chr14:g.93218529A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218529A>T , CM000676.2:g.93218529A>T	GRCh38
NC_000014.8:g.93684875A>T , CM000676.1:g.93684875A>T	GRCh37
NC_000014.7:g.92754628A>T	NCBI36
NG_051089.1:g.16474A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.604A>T MANE Select	ENSP00000013070.6:p.Thr202Ser
ENST00000013070.10:c.604A>T	ENSP00000013070.6:p.Thr202Ser
ENST00000416753.5:c.376A>T	ENSP00000391706.2:p.Thr126Ser
ENST00000553674.1:c.*305A>T	ENSP00000450470.1:n.*305A>T
ENST00000553857.5:c.378+3248A>T
ENST00000554232.5:c.508A>T	ENSP00000450645.1:p.Thr170Ser
ENST00000556871.5:c.313A>T	ENSP00000451022.1:p.Thr105Ser
ENST00000557048.1:n.513A>T
NM_175748.3:c.604A>T	NP_786924.2:p.Thr202Ser
NR_038150.1:n.706A>T
NM_175748.4:c.604A>T MANE Select	NP_786924.2:p.Thr202Ser
NR_038150.2:n.506A>T