Canonical Allele Identifier: CA1529373220
Gene: FBXL7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.15783391A= , CM000667.2:g.15783391A= GRCh38
NC_000005.9:g.15783500A= , CM000667.1:g.15783500A= GRCh37
NC_000005.8:g.15836500A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504595.2:c.128-144499A= MANE Select ENSP00000423630.1:n.128-144499A=
ENST00000504595.1:c.128-144499A= ENSP00000423630.1:n.128-144499A=
ENST00000510662.1:c.-14-144499A= ENSP00000425184.1:n.-14-144499A=
NM_001278317.1:c.-14-144499A= NP_001265246.1:n.-14-144499A=
NM_012304.4:c.128-144499A= NP_036436.1:n.128-144499A=
XM_005248273.3:c.113-144499A= XP_005248330.1:n.113-144499A=
XM_011513998.1:c.-91-51386A= XP_011512300.1:n.-91-51386A=
XM_017009262.2:c.113-144499A= XP_016864751.1:n.113-144499A=
NM_012304.5:c.128-144499A= MANE Select NP_036436.1:n.128-144499A=
NM_001278317.2:c.-14-144499A= NP_001265246.1:n.-14-144499A=