Canonical Allele Identifier: CA390810710

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93684899G>T (hg19) ; chr14:g.93218553G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218553G>T , CM000676.2:g.93218553G>T	GRCh38
NC_000014.8:g.93684899G>T , CM000676.1:g.93684899G>T	GRCh37
NC_000014.7:g.92754652G>T	NCBI36
NG_051089.1:g.16498G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.628G>T MANE Select	ENSP00000013070.6:p.Gly210Ter
ENST00000013070.10:c.628G>T	ENSP00000013070.6:p.Gly210Ter
ENST00000416753.5:c.400G>T	ENSP00000391706.2:p.Gly134Ter
ENST00000553674.1:c.*329G>T	ENSP00000450470.1:n.*329G>T
ENST00000553857.5:c.378+3272G>T
ENST00000554232.5:c.532G>T	ENSP00000450645.1:p.Gly178Ter
ENST00000556871.5:c.337G>T	ENSP00000451022.1:p.Gly113Ter
ENST00000557048.1:n.537G>T
NM_175748.3:c.628G>T	NP_786924.2:p.Gly210Ter
NR_038150.1:n.730G>T
NM_175748.4:c.628G>T MANE Select	NP_786924.2:p.Gly210Ter
NR_038150.2:n.530G>T