Canonical Allele Identifier: CA710048181

Gene: UBR7

Linked Data

• dbSNP Id: rs1183836769
• gnomAD v3: 14-93218421-AAAT-A
• gnomAD v4: 14-93218421-AAAT-A
• MyVariant Identifiers: chr14:g.93218422_93218424del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218432_93218434del , CM000676.2:g.93218432_93218434del	GRCh38
NC_000014.8:g.93684778_93684780del , CM000676.1:g.93684778_93684780del	GRCh37
NC_000014.7:g.92754531_92754533del	NCBI36
NG_051089.1:g.16377_16379del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-95_602-93del MANE Select	ENSP00000013070.6:n.602-95_602-93del
ENST00000013070.10:c.602-95_602-93del	ENSP00000013070.6:n.602-95_602-93del
ENST00000416753.5:c.374-95_374-93del	ENSP00000391706.2:n.374-95_374-93del
ENST00000553674.1:c.*303-95_*303-93del	ENSP00000450470.1:n.*303-95_*303-93del
ENST00000553857.5:c.378+3151_378+3153del
ENST00000554232.5:c.506-95_506-93del	ENSP00000450645.1:n.506-95_506-93del
ENST00000556871.5:c.311-95_311-93del	ENSP00000451022.1:n.311-95_311-93del
ENST00000557048.1:n.511-95_511-93del
NM_175748.3:c.602-95_602-93del	NP_786924.2:n.602-95_602-93del
NR_038150.1:n.704-95_704-93del
NM_175748.4:c.602-95_602-93del MANE Select	NP_786924.2:n.602-95_602-93del
NR_038150.2:n.504-95_504-93del