Canonical Allele Identifier: CA411329898

Gene: FBXO7

Linked Data

• MyVariant Identifiers: chr22:g.32871042A>T (hg19) ; chr22:g.32475055A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32475055A>T , CM000684.2:g.32475055A>T	GRCh38
NC_000022.10:g.32871042A>T , CM000684.1:g.32871042A>T	GRCh37
NC_000022.9:g.31201042A>T	NCBI36
NG_016001.1:g.5336A>T
NG_016001.2:g.5336A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.53A>T MANE Select	ENSP00000266087.7:p.Glu18Val
ENST00000266087.11:c.53A>T	ENSP00000266087.7:p.Glu18Val
ENST00000420700.5:c.53A>T	ENSP00000406155.1:p.Glu18Val
ENST00000425028.5:c.53A>T	ENSP00000395823.1:p.Glu18Val
ENST00000492535.1:n.41A>T
NM_012179.3:c.53A>T	NP_036311.3:p.Glu18Val
XM_011530106.1:c.-121A>T	XP_011528408.1:n.-121A>T
XM_024452207.1:c.-138A>T	XP_024307975.1:n.-138A>T
NM_012179.4:c.53A>T MANE Select	NP_036311.3:p.Glu18Val