Canonical Allele Identifier: CA2466653292

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353353G= , CM000685.2:g.154353353G=	GRCh38
NC_000023.10:g.153581721G= , CM000685.1:g.153581721G=	GRCh37
NC_000023.9:g.153234915G=	NCBI36
NG_011506.1:g.26286C=
NG_011506.2:g.26286C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5941C=	ENSP00000353467.4:p.Pro1981=
ENST00000369850.10:c.5965C= MANE Select	ENSP00000358866.3:p.Pro1989=
ENST00000369856.8:c.5884C=	ENSP00000358872.4:p.Pro1962=
ENST00000422373.6:c.3161-678C=	ENSP00000416926.2:n.3161-678C=
ENST00000610817.5:c.6022C=	ENSP00000480593.2:n.6022C=
ENST00000673639.2:c.280-4663C=
ENST00000676696.1:c.6244C=	ENSP00000503392.1:n.6244C=
ENST00000678304.1:n.1144C=
ENST00000344736.8:c.5845C=	ENSP00000358863.3:p.Pro1949=
ENST00000360319.8:c.5941C=	ENSP00000353467.4:p.Pro1981=
ENST00000369850.7:c.5965C=	ENSP00000358866.3:p.Pro1989=
ENST00000369856.7:c.5884C=	ENSP00000358872.4:p.Pro1962=
ENST00000415241.1:c.150C=
ENST00000420627.5:c.5921C=	ENSP00000408921.1:n.5921C=
ENST00000422373.5:c.5941C=	ENSP00000416926.1:p.Pro1981=
ENST00000438732.2:c.639C=
ENST00000466325.1:n.104C=
ENST00000490936.5:n.1954C=
ENST00000610817.4:c.5844+40C=	ENSP00000480593.1:n.5844+40C=
NM_001110556.1:c.5965C=	NP_001104026.1:p.Pro1989=
NM_001456.3:c.5941C=	NP_001447.2:p.Pro1981=
XM_011531127.1:c.5869C=	XP_011529429.1:p.Pro1957=
XM_011531128.1:c.5845C=	XP_011529430.1:p.Pro1949=
XM_011531129.1:c.5791C=	XP_011529431.1:p.Pro1931=
XM_011531130.1:c.5767C=	XP_011529432.1:p.Pro1923=
XM_011531131.1:c.5764C=	XP_011529433.1:p.Pro1922=
NM_001110556.2:c.5965C= MANE Select	NP_001104026.1:p.Pro1989=
NM_001456.4:c.5941C=	NP_001447.2:p.Pro1981=