Canonical Allele Identifier: CA1529373258

Gene: FBXL7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15783468C= , CM000667.2:g.15783468C=	GRCh38
NC_000005.9:g.15783577C= , CM000667.1:g.15783577C=	GRCh37
NC_000005.8:g.15836577C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000504595.2:c.128-144422C= MANE Select	ENSP00000423630.1:n.128-144422C=
ENST00000504595.1:c.128-144422C=	ENSP00000423630.1:n.128-144422C=
ENST00000510662.1:c.-14-144422C=	ENSP00000425184.1:n.-14-144422C=
NM_001278317.1:c.-14-144422C=	NP_001265246.1:n.-14-144422C=
NM_012304.4:c.128-144422C=	NP_036436.1:n.128-144422C=
XM_005248273.3:c.113-144422C=	XP_005248330.1:n.113-144422C=
XM_011513998.1:c.-91-51309C=	XP_011512300.1:n.-91-51309C=
XM_017009262.2:c.113-144422C=	XP_016864751.1:n.113-144422C=
NM_012304.5:c.128-144422C= MANE Select	NP_036436.1:n.128-144422C=
NM_001278317.2:c.-14-144422C=	NP_001265246.1:n.-14-144422C=