Canonical Allele Identifier: CA411329838

Gene: FBXO7

Linked Data

• MyVariant Identifiers: chr22:g.32871014A>T (hg19) ; chr22:g.32475027A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.32475027A>T , CM000684.2:g.32475027A>T	GRCh38
NC_000022.10:g.32871014A>T , CM000684.1:g.32871014A>T	GRCh37
NC_000022.9:g.31201014A>T	NCBI36
NG_016001.1:g.5308A>T
NG_016001.2:g.5308A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266087.12:c.25A>T MANE Select	ENSP00000266087.7:p.Lys9Ter
ENST00000266087.11:c.25A>T	ENSP00000266087.7:p.Lys9Ter
ENST00000420700.5:c.25A>T	ENSP00000406155.1:p.Lys9Ter
ENST00000425028.5:c.25A>T	ENSP00000395823.1:p.Lys9Ter
ENST00000492535.1:n.13A>T
NM_012179.3:c.25A>T	NP_036311.3:p.Lys9Ter
XM_011530106.1:c.-149A>T	XP_011528408.1:n.-149A>T
XM_024452207.1:c.-166A>T	XP_024307975.1:n.-166A>T
NM_012179.4:c.25A>T MANE Select	NP_036311.3:p.Lys9Ter