Canonical Allele Identifier: CA8612859
Gene: FMNL1 HGNC NCBI
FMNL1-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45241616A>C , CM000679.2:g.45241616A>C GRCh38
NC_000017.10:g.43318983A>C , CM000679.1:g.43318983A>C GRCh37
NC_000017.9:g.40674766A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000587489.6:c.1567A>C (FMNL1) ENSP00000465474.2:p.Thr523Pro
ENST00000331495.8:c.1567A>C (FMNL1) MANE Select ENSP00000329219.2:p.Thr523Pro
ENST00000328118.7:c.721A>C (FMNL1) ENSP00000327442.4:p.Thr241Pro
ENST00000331495.7:c.1567A>C (FMNL1) ENSP00000329219.2:p.Thr523Pro
ENST00000587489.5:c.301A>C (FMNL1) ENSP00000465474.1:p.Thr101Pro
ENST00000587856.1:n.1924A>C (FMNL1)
NM_005892.3:c.1567A>C (FMNL1) NP_005883.2:p.Thr523Pro
XM_006722062.2:c.1585A>C (FMNL1) XP_006722125.1:p.Thr529Pro
XM_006722063.2:c.1567A>C (FMNL1) XP_006722126.1:p.Thr523Pro
XM_006722064.2:c.1555A>C (FMNL1) XP_006722127.1:p.Thr519Pro
XM_006722065.2:c.1537A>C (FMNL1) XP_006722128.1:p.Thr513Pro
XM_006722066.2:c.1585A>C (FMNL1) XP_006722129.1:p.Thr529Pro
XM_006722069.1:c.1585A>C (FMNL1) XP_006722132.1:p.Thr529Pro
XM_006722070.2:c.1567A>C (FMNL1) XP_006722133.1:p.Thr523Pro
XM_011525179.1:c.1585A>C (FMNL1) XP_011523481.1:p.Thr529Pro
XM_011525180.1:c.1492A>C (FMNL1) XP_011523482.1:p.Thr498Pro
XM_011525181.1:c.1585A>C (FMNL1) XP_011523483.1:p.Thr529Pro
XM_011525182.1:c.1585A>C (FMNL1) XP_011523484.1:p.Thr529Pro
XM_006722062.4:c.1585A>C (FMNL1) XP_006722125.1:p.Thr529Pro
XM_006722063.4:c.1567A>C (FMNL1) XP_006722126.1:p.Thr523Pro
XM_006722064.4:c.1555A>C (FMNL1) XP_006722127.1:p.Thr519Pro
XM_006722065.4:c.1537A>C (FMNL1) XP_006722128.1:p.Thr513Pro
XM_006722066.4:c.1585A>C (FMNL1) XP_006722129.1:p.Thr529Pro
XM_006722069.3:c.1585A>C (FMNL1) XP_006722132.1:p.Thr529Pro
XM_006722070.4:c.1567A>C (FMNL1) XP_006722133.1:p.Thr523Pro
XM_011525179.3:c.1585A>C (FMNL1) XP_011523481.1:p.Thr529Pro
XM_011525180.2:c.1492A>C (FMNL1) XP_011523482.1:p.Thr498Pro
XM_011525182.3:c.1585A>C (FMNL1) XP_011523484.1:p.Thr529Pro
XR_001752908.2:n.253T>G (FMNL1-AS1)
NM_005892.4:c.1567A>C (FMNL1) MANE Select NP_005883.3:p.Thr523Pro