Canonical Allele Identifier: CA399877744

Gene: FMNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45244176C>G , CM000679.2:g.45244176C>G	GRCh38
NC_000017.10:g.43321543C>G , CM000679.1:g.43321543C>G	GRCh37
NC_000017.9:g.40677326C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587489.6:c.2449C>G	ENSP00000465474.2:p.Gln817Glu
ENST00000331495.8:c.2449C>G MANE Select	ENSP00000329219.2:p.Gln817Glu
ENST00000328118.7:c.1414C>G	ENSP00000327442.4:p.Gln472Glu
ENST00000331495.7:c.2449C>G	ENSP00000329219.2:p.Gln817Glu
ENST00000586643.5:c.439C>G	ENSP00000465137.1:p.Gln147Glu
ENST00000587489.5:c.1183C>G	ENSP00000465474.1:p.Gln395Glu
ENST00000587856.1:n.3168C>G
NM_005892.3:c.2449C>G	NP_005883.2:p.Gln817Glu
XM_006722062.2:c.2467C>G	XP_006722125.1:p.Gln823Glu
XM_006722063.2:c.2449C>G	XP_006722126.1:p.Gln817Glu
XM_006722064.2:c.2437C>G	XP_006722127.1:p.Gln813Glu
XM_006722065.2:c.2419C>G	XP_006722128.1:p.Gln807Glu
XM_006722066.2:c.2467C>G	XP_006722129.1:p.Gln823Glu
XM_006722069.1:c.2467C>G	XP_006722132.1:p.Gln823Glu
XM_006722070.2:c.2449C>G	XP_006722133.1:p.Gln817Glu
XM_011525179.1:c.2467C>G	XP_011523481.1:p.Gln823Glu
XM_011525180.1:c.2374C>G	XP_011523482.1:p.Gln792Glu
XM_011525181.1:c.2467C>G	XP_011523483.1:p.Gln823Glu
XM_011525182.1:c.2467C>G	XP_011523484.1:p.Gln823Glu
XM_006722062.4:c.2467C>G	XP_006722125.1:p.Gln823Glu
XM_006722063.4:c.2449C>G	XP_006722126.1:p.Gln817Glu
XM_006722064.4:c.2437C>G	XP_006722127.1:p.Gln813Glu
XM_006722065.4:c.2419C>G	XP_006722128.1:p.Gln807Glu
XM_006722066.4:c.2467C>G	XP_006722129.1:p.Gln823Glu
XM_006722069.3:c.2467C>G	XP_006722132.1:p.Gln823Glu
XM_006722070.4:c.2449C>G	XP_006722133.1:p.Gln817Glu
XM_011525179.3:c.2467C>G	XP_011523481.1:p.Gln823Glu
XM_011525180.2:c.2374C>G	XP_011523482.1:p.Gln792Glu
XM_011525182.3:c.2467C>G	XP_011523484.1:p.Gln823Glu
NM_005892.4:c.2449C>G MANE Select	NP_005883.3:p.Gln817Glu