Canonical Allele Identifier: CA806023892

Gene: FBXL7

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.15581896T>C , CM000667.2:g.15581896T>C	GRCh38
NC_000005.9:g.15582005T>C , CM000667.1:g.15582005T>C	GRCh37
NC_000005.8:g.15635005T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504595.2:c.38-34087T>C MANE Select	ENSP00000423630.1:n.38-34087T>C
ENST00000504595.1:c.38-34087T>C	ENSP00000423630.1:n.38-34087T>C
ENST00000510662.1:c.-104-34087T>C	ENSP00000425184.1:n.-104-34087T>C
NM_001278317.1:c.-104-34087T>C	NP_001265246.1:n.-104-34087T>C
NM_012304.4:c.38-34087T>C	NP_036436.1:n.38-34087T>C
XM_005248273.3:c.22+1084T>C	XP_005248330.1:n.22+1084T>C
XM_017009262.2:c.22+1084T>C	XP_016864751.1:n.22+1084T>C
NM_012304.5:c.38-34087T>C MANE Select	NP_036436.1:n.38-34087T>C
NM_001278317.2:c.-104-34087T>C	NP_001265246.1:n.-104-34087T>C