Canonical Allele Identifier: CA415182895

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154349822C>T , CM000685.2:g.154349822C>T	GRCh38
NC_000023.10:g.153578190C>T , CM000685.1:g.153578190C>T	GRCh37
NC_000023.9:g.153231384C>T	NCBI36
NG_011506.1:g.29817G>A
NG_011506.2:g.29817G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.7379G>A MANE Select	NP_001104026.1:p.Gly2460Asp
ENST00000369850.10:c.7379G>A MANE Select	ENSP00000358866.3:p.Gly2460Asp
NM_001110556.1:c.7379G>A	NP_001104026.1:p.Gly2460Asp
NM_001456.3:c.7355G>A	NP_001447.2:p.Gly2452Asp
NM_001456.4:c.7355G>A	NP_001447.2:p.Gly2452Asp
ENST00000344736.8:c.7259G>A	ENSP00000358863.3:p.Gly2420Asp
ENST00000360319.8:c.7355G>A	ENSP00000353467.4:p.Gly2452Asp
ENST00000360319.9:c.7355G>A	ENSP00000353467.4:p.Gly2452Asp
ENST00000369850.7:c.7379G>A	ENSP00000358866.3:p.Gly2460Asp
ENST00000369856.7:c.7298G>A	ENSP00000358872.4:p.Gly2433Asp
ENST00000369856.8:c.7298G>A	ENSP00000358872.4:p.Gly2433Asp
ENST00000420627.5:c.7335G>A	ENSP00000408921.1:n.7335G>A
ENST00000422373.5:c.7355G>A	ENSP00000416926.1:p.Gly2452Asp
ENST00000422373.6:c.4160G>A	ENSP00000416926.2:p.Gly1387Asp
ENST00000462590.1:n.534G>A
ENST00000490936.5:n.4608G>A
ENST00000498411.1:n.68-992G>A
ENST00000498491.5:n.420G>A
ENST00000610817.4:c.6383G>A	ENSP00000480593.1:p.Gly2128Asp
ENST00000610817.5:c.7436G>A	ENSP00000480593.2:n.7436G>A
ENST00000673639.2:c.280-1132G>A
ENST00000676696.1:c.7658G>A	ENSP00000503392.1:n.7658G>A
ENST00000678304.1:n.3097G>A
XM_011531127.1:c.7283G>A	XP_011529429.1:p.Gly2428Asp
XM_011531128.1:c.7259G>A	XP_011529430.1:p.Gly2420Asp
XM_011531129.1:c.7205G>A	XP_011529431.1:p.Gly2402Asp
XM_011531130.1:c.7181G>A	XP_011529432.1:p.Gly2394Asp
XM_011531131.1:c.7178G>A	XP_011529433.1:p.Gly2393Asp