Canonical Allele Identifier: CA337275561

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353452C>T , CM000685.2:g.154353452C>T	GRCh38
NC_000023.10:g.153581820C>T , CM000685.1:g.153581820C>T	GRCh37
NC_000023.9:g.153235014C>T	NCBI36
NG_011506.1:g.26187G>A
NG_011506.2:g.26187G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.5866G>A MANE Select	NP_001104026.1:p.Asp1956Asn
ENST00000369850.10:c.5866G>A MANE Select	ENSP00000358866.3:p.Asp1956Asn
NM_001110556.1:c.5866G>A	NP_001104026.1:p.Asp1956Asn
NM_001456.3:c.5842G>A	NP_001447.2:p.Asp1948Asn
NM_001456.4:c.5842G>A	NP_001447.2:p.Asp1948Asn
ENST00000344736.8:c.5746G>A	ENSP00000358863.3:p.Asp1916Asn
ENST00000360319.8:c.5842G>A	ENSP00000353467.4:p.Asp1948Asn
ENST00000360319.9:c.5842G>A	ENSP00000353467.4:p.Asp1948Asn
ENST00000369850.7:c.5866G>A	ENSP00000358866.3:p.Asp1956Asn
ENST00000369856.7:c.5785G>A	ENSP00000358872.4:p.Asp1929Asn
ENST00000369856.8:c.5785G>A	ENSP00000358872.4:p.Asp1929Asn
ENST00000415241.1:c.51G>A
ENST00000420627.5:c.5822G>A	ENSP00000408921.1:n.5822G>A
ENST00000422373.5:c.5842G>A	ENSP00000416926.1:p.Asp1948Asn
ENST00000422373.6:c.3161-777G>A	ENSP00000416926.2:n.3161-777G>A
ENST00000438732.2:c.540G>A
ENST00000466325.1:n.5G>A
ENST00000490936.5:n.1855G>A
ENST00000610817.4:c.5785G>A	ENSP00000480593.1:p.Asp1929Asn
ENST00000610817.5:c.5923G>A	ENSP00000480593.2:n.5923G>A
ENST00000673639.2:c.280-4762G>A
ENST00000676696.1:c.6145G>A	ENSP00000503392.1:n.6145G>A
ENST00000678304.1:n.1045G>A
XM_011531127.1:c.5770G>A	XP_011529429.1:p.Asp1924Asn
XM_011531128.1:c.5746G>A	XP_011529430.1:p.Asp1916Asn
XM_011531129.1:c.5692G>A	XP_011529431.1:p.Asp1898Asn
XM_011531130.1:c.5668G>A	XP_011529432.1:p.Asp1890Asn
XM_011531131.1:c.5665G>A	XP_011529433.1:p.Asp1889Asn