Canonical Allele Identifier: CA10201567

Gene: FBXO7

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32491079A>T , CM000684.2:g.32491079A>T	GRCh38
NC_000022.10:g.32887066A>T , CM000684.1:g.32887066A>T	GRCh37
NC_000022.9:g.31217066A>T	NCBI36
NG_016001.1:g.21360A>T
NG_016001.2:g.21360A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_012179.4:c.872-7A>T MANE Select	NP_036311.3:n.872-7A>T
ENST00000266087.12:c.872-7A>T MANE Select	ENSP00000266087.7:n.872-7A>T
NM_001033024.1:c.635-7A>T	NP_001028196.1:n.635-7A>T
NM_001033024.2:c.635-7A>T	NP_001028196.1:n.635-7A>T
NM_001257990.1:c.530-7A>T	NP_001244919.1:n.530-7A>T
NM_001257990.2:c.530-7A>T	NP_001244919.1:n.530-7A>T
NM_012179.3:c.872-7A>T	NP_036311.3:n.872-7A>T
ENST00000266087.11:c.872-7A>T	ENSP00000266087.7:n.872-7A>T
ENST00000397426.5:c.530-7A>T	ENSP00000380571.1:n.530-7A>T
ENST00000420700.5:c.*451-7A>T	ENSP00000406155.1:n.*451-7A>T
ENST00000425028.5:c.*570-7A>T	ENSP00000395823.1:n.*570-7A>T
ENST00000452138.3:c.635-7A>T	ENSP00000388547.2:n.635-7A>T
ENST00000484607.1:n.542-7A>T
ENST00000492535.1:n.3958A>T
XM_011530106.1:c.404-7A>T	XP_011528408.1:n.404-7A>T
XM_024452207.1:c.530-7A>T	XP_024307975.1:n.530-7A>T