Canonical Allele Identifier: CA2501691535

Gene: FBXO7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32474940_32474967del , CM000684.2:g.32474940_32474967del	GRCh38
NC_000022.10:g.32870927_32870954del , CM000684.1:g.32870927_32870954del	GRCh37
NC_000022.9:g.31200927_31200954del	NCBI36
NG_016001.1:g.5221_5248del
NG_016001.2:g.5221_5248del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.-63_-36del MANE Select	ENSP00000266087.7:n.-63_-36del
ENST00000266087.11:c.-63_-36del	ENSP00000266087.7:n.-63_-36del
ENST00000420700.5:c.-63_-36del	ENSP00000406155.1:n.-63_-36del
ENST00000425028.5:c.-63_-36del	ENSP00000395823.1:n.-63_-36del
NM_012179.3:c.-63_-36del	NP_036311.3:n.-63_-36del
XM_011530106.1:c.-236_-209del	XP_011528408.1:n.-236_-209del
XM_024452207.1:c.-253_-226del	XP_024307975.1:n.-253_-226del
NM_012179.4:c.-63_-36del MANE Select	NP_036311.3:n.-63_-36del