Canonical Allele Identifier: CA710048202

Gene: UBR7

Linked Data

• dbSNP Id: rs1220293370
• MyVariant Identifiers: chr14:g.93218443_93218460del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218455_93218472del , CM000676.2:g.93218455_93218472del	GRCh38
NC_000014.8:g.93684801_93684818del , CM000676.1:g.93684801_93684818del	GRCh37
NC_000014.7:g.92754554_92754571del	NCBI36
NG_051089.1:g.16400_16417del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-72_602-55del MANE Select	ENSP00000013070.6:n.602-72_602-55del
ENST00000013070.10:c.602-72_602-55del	ENSP00000013070.6:n.602-72_602-55del
ENST00000416753.5:c.374-72_374-55del	ENSP00000391706.2:n.374-72_374-55del
ENST00000553674.1:c.*303-72_*303-55del	ENSP00000450470.1:n.*303-72_*303-55del
ENST00000553857.5:c.378+3174_378+3191del
ENST00000554232.5:c.506-72_506-55del	ENSP00000450645.1:n.506-72_506-55del
ENST00000556871.5:c.311-72_311-55del	ENSP00000451022.1:n.311-72_311-55del
ENST00000557048.1:n.511-72_511-55del
NM_175748.3:c.602-72_602-55del	NP_786924.2:n.602-72_602-55del
NR_038150.1:n.704-72_704-55del
NM_175748.4:c.602-72_602-55del MANE Select	NP_786924.2:n.602-72_602-55del
NR_038150.2:n.504-72_504-55del