Canonical Allele Identifier: CA399876094

Gene: FMNL1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45243214G>C , CM000679.2:g.45243214G>C	GRCh38
NC_000017.10:g.43320581G>C , CM000679.1:g.43320581G>C	GRCh37
NC_000017.9:g.40676364G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587489.6:c.2107G>C	ENSP00000465474.2:p.Ala703Pro
ENST00000331495.8:c.2107G>C MANE Select	ENSP00000329219.2:p.Ala703Pro
ENST00000328118.7:c.1072G>C	ENSP00000327442.4:p.Ala358Pro
ENST00000331495.7:c.2107G>C	ENSP00000329219.2:p.Ala703Pro
ENST00000586643.5:c.97G>C	ENSP00000465137.1:p.Ala33Pro
ENST00000587489.5:c.841G>C	ENSP00000465474.1:p.Ala281Pro
ENST00000587856.1:n.2676G>C
NM_005892.3:c.2107G>C	NP_005883.2:p.Ala703Pro
XM_006722062.2:c.2125G>C	XP_006722125.1:p.Ala709Pro
XM_006722063.2:c.2107G>C	XP_006722126.1:p.Ala703Pro
XM_006722064.2:c.2095G>C	XP_006722127.1:p.Ala699Pro
XM_006722065.2:c.2077G>C	XP_006722128.1:p.Ala693Pro
XM_006722066.2:c.2125G>C	XP_006722129.1:p.Ala709Pro
XM_006722069.1:c.2125G>C	XP_006722132.1:p.Ala709Pro
XM_006722070.2:c.2107G>C	XP_006722133.1:p.Ala703Pro
XM_011525179.1:c.2125G>C	XP_011523481.1:p.Ala709Pro
XM_011525180.1:c.2032G>C	XP_011523482.1:p.Ala678Pro
XM_011525181.1:c.2125G>C	XP_011523483.1:p.Ala709Pro
XM_011525182.1:c.2125G>C	XP_011523484.1:p.Ala709Pro
XM_006722062.4:c.2125G>C	XP_006722125.1:p.Ala709Pro
XM_006722063.4:c.2107G>C	XP_006722126.1:p.Ala703Pro
XM_006722064.4:c.2095G>C	XP_006722127.1:p.Ala699Pro
XM_006722065.4:c.2077G>C	XP_006722128.1:p.Ala693Pro
XM_006722066.4:c.2125G>C	XP_006722129.1:p.Ala709Pro
XM_006722069.3:c.2125G>C	XP_006722132.1:p.Ala709Pro
XM_006722070.4:c.2107G>C	XP_006722133.1:p.Ala703Pro
XM_011525179.3:c.2125G>C	XP_011523481.1:p.Ala709Pro
XM_011525180.2:c.2032G>C	XP_011523482.1:p.Ala678Pro
XM_011525182.3:c.2125G>C	XP_011523484.1:p.Ala709Pro
NM_005892.4:c.2107G>C MANE Select	NP_005883.3:p.Ala703Pro