Canonical Allele Identifier: CA1529373474
Gene: FBXL7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.15783913C= , CM000667.2:g.15783913C= GRCh38
NC_000005.9:g.15784022C= , CM000667.1:g.15784022C= GRCh37
NC_000005.8:g.15837022C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000504595.2:c.128-143977C= MANE Select ENSP00000423630.1:n.128-143977C=
ENST00000504595.1:c.128-143977C= ENSP00000423630.1:n.128-143977C=
ENST00000510662.1:c.-14-143977C= ENSP00000425184.1:n.-14-143977C=
NM_001278317.1:c.-14-143977C= NP_001265246.1:n.-14-143977C=
NM_012304.4:c.128-143977C= NP_036436.1:n.128-143977C=
XM_005248273.3:c.113-143977C= XP_005248330.1:n.113-143977C=
XM_011513998.1:c.-91-50864C= XP_011512300.1:n.-91-50864C=
XM_017009262.2:c.113-143977C= XP_016864751.1:n.113-143977C=
NM_012304.5:c.128-143977C= MANE Select NP_036436.1:n.128-143977C=
NM_001278317.2:c.-14-143977C= NP_001265246.1:n.-14-143977C=