Canonical Allele Identifier: CA487593972

Gene: UBR7

Linked Data

• dbSNP Id: rs1402438031
• MyVariant Identifiers: chr14:g.93684764_93684765insAAT (hg19) ; chr14:g.93218418_93218419insAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.93218420_93218421insTAA , CM000676.2:g.93218420_93218421insTAA	GRCh38
NC_000014.8:g.93684766_93684767insTAA , CM000676.1:g.93684766_93684767insTAA	GRCh37
NC_000014.7:g.92754519_92754520insTAA	NCBI36
NG_051089.1:g.16365_16366insTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000013070.11:c.602-107_602-106insTAA MANE Select	ENSP00000013070.6:n.602-107_602-106insTAA
ENST00000013070.10:c.602-107_602-106insTAA	ENSP00000013070.6:n.602-107_602-106insTAA
ENST00000416753.5:c.374-107_374-106insTAA	ENSP00000391706.2:n.374-107_374-106insTAA
ENST00000553674.1:c.*303-107_*303-106insTAA	ENSP00000450470.1:n.*303-107_*303-106insTAA
ENST00000553857.5:c.378+3139_378+3140insTAA
ENST00000554232.5:c.506-107_506-106insTAA	ENSP00000450645.1:n.506-107_506-106insTAA
ENST00000556871.5:c.311-107_311-106insTAA	ENSP00000451022.1:n.311-107_311-106insTAA
ENST00000557048.1:n.511-107_511-106insTAA
NM_175748.3:c.602-107_602-106insTAA	NP_786924.2:n.602-107_602-106insTAA
NR_038150.1:n.704-107_704-106insTAA
NM_175748.4:c.602-107_602-106insTAA MANE Select	NP_786924.2:n.602-107_602-106insTAA
NR_038150.2:n.504-107_504-106insTAA