Canonical Allele Identifier: CA1529373214
Gene: FBXL7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.15783388G= , CM000667.2:g.15783388G= GRCh38
NC_000005.9:g.15783497G= , CM000667.1:g.15783497G= GRCh37
NC_000005.8:g.15836497G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000504595.2:c.128-144502G= MANE Select ENSP00000423630.1:n.128-144502G=
ENST00000504595.1:c.128-144502G= ENSP00000423630.1:n.128-144502G=
ENST00000510662.1:c.-14-144502G= ENSP00000425184.1:n.-14-144502G=
NM_001278317.1:c.-14-144502G= NP_001265246.1:n.-14-144502G=
NM_012304.4:c.128-144502G= NP_036436.1:n.128-144502G=
XM_005248273.3:c.113-144502G= XP_005248330.1:n.113-144502G=
XM_011513998.1:c.-91-51389G= XP_011512300.1:n.-91-51389G=
XM_017009262.2:c.113-144502G= XP_016864751.1:n.113-144502G=
NM_012304.5:c.128-144502G= MANE Select NP_036436.1:n.128-144502G=
NM_001278317.2:c.-14-144502G= NP_001265246.1:n.-14-144502G=