Canonical Allele Identifier: CA399882374

Gene: FMNL1 EFCAB15P

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45246217C>T , CM000679.2:g.45246217C>T	GRCh38
NC_000017.10:g.43323584C>T , CM000679.1:g.43323584C>T	GRCh37
NC_000017.9:g.40679367C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000587489.6:c.3098C>T (FMNL1)	ENSP00000465474.2:p.Pro1033Leu
ENST00000331495.8:c.3098C>T (FMNL1) MANE Select	ENSP00000329219.2:p.Pro1033Leu
ENST00000420431.2:n.466-918G>A (EFCAB15P)
ENST00000328118.7:c.*195C>T (FMNL1)	ENSP00000327442.4:n.*195C>T
ENST00000331495.7:c.3098C>T (FMNL1)	ENSP00000329219.2:p.Pro1033Leu
ENST00000586092.1:c.195C>T (FMNL1)
ENST00000586643.5:c.1088C>T (FMNL1)	ENSP00000465137.1:p.Pro363Leu
ENST00000587489.5:c.1832C>T (FMNL1)	ENSP00000465474.1:p.Pro611Leu
ENST00000587856.1:n.3817C>T (FMNL1)
ENST00000589911.1:c.433C>T (FMNL1)	ENSP00000466711.1:n.433C>T
NM_005892.3:c.3098C>T (FMNL1)	NP_005883.2:p.Pro1033Leu
XM_006722062.2:c.3116C>T (FMNL1)	XP_006722125.1:p.Pro1039Leu
XM_006722063.2:c.3098C>T (FMNL1)	XP_006722126.1:p.Pro1033Leu
XM_006722064.2:c.3086C>T (FMNL1)	XP_006722127.1:p.Pro1029Leu
XM_006722065.2:c.3068C>T (FMNL1)	XP_006722128.1:p.Pro1023Leu
XM_006722066.2:c.3116C>T (FMNL1)	XP_006722129.1:p.Pro1039Leu
XM_006722069.1:c.3014C>T (FMNL1)	XP_006722132.1:p.Pro1005Leu
XM_006722070.2:c.3098C>T (FMNL1)	XP_006722133.1:p.Pro1033Leu
XM_011525179.1:c.3116C>T (FMNL1)	XP_011523481.1:p.Pro1039Leu
XM_011525180.1:c.3023C>T (FMNL1)	XP_011523482.1:p.Pro1008Leu
XM_011525181.1:c.3014C>T (FMNL1)	XP_011523483.1:p.Pro1005Leu
XM_011525182.1:c.3116C>T (FMNL1)	XP_011523484.1:p.Pro1039Leu
XM_006722062.4:c.3116C>T (FMNL1)	XP_006722125.1:p.Pro1039Leu
XM_006722063.4:c.3098C>T (FMNL1)	XP_006722126.1:p.Pro1033Leu
XM_006722064.4:c.3086C>T (FMNL1)	XP_006722127.1:p.Pro1029Leu
XM_006722065.4:c.3068C>T (FMNL1)	XP_006722128.1:p.Pro1023Leu
XM_006722066.4:c.3116C>T (FMNL1)	XP_006722129.1:p.Pro1039Leu
XM_006722069.3:c.3014C>T (FMNL1)	XP_006722132.1:p.Pro1005Leu
XM_006722070.4:c.3098C>T (FMNL1)	XP_006722133.1:p.Pro1033Leu
XM_011525179.3:c.3116C>T (FMNL1)	XP_011523481.1:p.Pro1039Leu
XM_011525180.2:c.3023C>T (FMNL1)	XP_011523482.1:p.Pro1008Leu
XM_011525182.3:c.3116C>T (FMNL1)	XP_011523484.1:p.Pro1039Leu
NM_005892.4:c.3098C>T (FMNL1) MANE Select	NP_005883.3:p.Pro1033Leu