Canonical Allele Identifier: CA1571013823
Gene: FBXL17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.107945861C= , CM000667.2:g.107945861C= GRCh38
NC_000005.9:g.107281562C= , CM000667.1:g.107281562C= GRCh37
NC_000005.8:g.107309461C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000496714.2:c.831-64682G=
ENST00000542267.7:c.1823-64682G= MANE Select ENSP00000437464.2:n.1823-64682G=
ENST00000359660.9:c.629-64682G= ENSP00000352683.4:n.629-64682G=
ENST00000496714.1:c.629-64682G= ENSP00000418111.1:n.629-64682G=
ENST00000542267.5:c.1823-64682G= ENSP00000437464.1:n.1823-64682G=
ENST00000619412.4:c.1109-64682G= ENSP00000481439.1:n.1109-64682G=
NM_001163315.2:c.1823-64682G= NP_001156787.2:n.1823-64682G=
XM_005272048.3:c.1823-64682G= XP_005272105.1:n.1823-64682G=
XM_005272048.4:c.1823-64682G= XP_005272105.1:n.1823-64682G=
NM_001163315.3:c.1823-64682G= MANE Select NP_001156787.2:n.1823-64682G=