Canonical Allele Identifier: CA390811114

Gene: UBR7

Linked Data

• MyVariant Identifiers: chr14:g.93685007G>T (hg19) ; chr14:g.93218661G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218661G>T , CM000676.2:g.93218661G>T	GRCh38
NC_000014.8:g.93685007G>T , CM000676.1:g.93685007G>T	GRCh37
NC_000014.7:g.92754760G>T	NCBI36
NG_051089.1:g.16606G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000013070.11:c.736G>T MANE Select	ENSP00000013070.6:p.Asp246Tyr
ENST00000013070.10:c.736G>T	ENSP00000013070.6:p.Asp246Tyr
ENST00000416753.5:c.508G>T	ENSP00000391706.2:p.Asp170Tyr
ENST00000553674.1:c.*437G>T	ENSP00000450470.1:n.*437G>T
ENST00000553857.5:c.378+3380G>T
ENST00000556871.5:c.445G>T	ENSP00000451022.1:p.Asp149Tyr
NM_175748.3:c.736G>T	NP_786924.2:p.Asp246Tyr
NR_038150.1:n.838G>T
NM_175748.4:c.736G>T MANE Select	NP_786924.2:p.Asp246Tyr
NR_038150.2:n.638G>T