Canonical Allele Identifier: CA202917

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350142C>T , CM000685.2:g.154350142C>T	GRCh38
NC_000023.10:g.153578510C>T , CM000685.1:g.153578510C>T	GRCh37
NC_000023.9:g.153231704C>T	NCBI36
NG_011506.1:g.29497G>A
NG_011506.2:g.29497G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7198G>A	ENSP00000353467.4:p.Gly2400Ser
ENST00000369850.10:c.7222G>A MANE Select	ENSP00000358866.3:p.Gly2408Ser
ENST00000369856.8:c.7141G>A	ENSP00000358872.4:p.Gly2381Ser
ENST00000422373.6:c.4003G>A	ENSP00000416926.2:p.Gly1335Ser
ENST00000610817.5:c.7279G>A	ENSP00000480593.2:n.7279G>A
ENST00000673639.2:c.280-1452G>A
ENST00000676696.1:c.7501G>A	ENSP00000503392.1:n.7501G>A
ENST00000678304.1:n.2940G>A
ENST00000344736.8:c.7102G>A	ENSP00000358863.3:p.Gly2368Ser
ENST00000360319.8:c.7198G>A	ENSP00000353467.4:p.Gly2400Ser
ENST00000369850.7:c.7222G>A	ENSP00000358866.3:p.Gly2408Ser
ENST00000369856.7:c.7141G>A	ENSP00000358872.4:p.Gly2381Ser
ENST00000420627.5:c.7178G>A	ENSP00000408921.1:n.7178G>A
ENST00000422373.5:c.7198G>A	ENSP00000416926.1:p.Gly2400Ser
ENST00000462590.1:n.214G>A
ENST00000490936.5:n.4451G>A
ENST00000498411.1:n.68-1312G>A
ENST00000498491.5:n.263G>A
ENST00000610817.4:c.6226G>A	ENSP00000480593.1:p.Gly2076Ser
NM_001110556.1:c.7222G>A	NP_001104026.1:p.Gly2408Ser
NM_001456.3:c.7198G>A	NP_001447.2:p.Gly2400Ser
XM_011531127.1:c.7126G>A	XP_011529429.1:p.Gly2376Ser
XM_011531128.1:c.7102G>A	XP_011529430.1:p.Gly2368Ser
XM_011531129.1:c.7048G>A	XP_011529431.1:p.Gly2350Ser
XM_011531130.1:c.7024G>A	XP_011529432.1:p.Gly2342Ser
XM_011531131.1:c.7021G>A	XP_011529433.1:p.Gly2341Ser
NM_001110556.2:c.7222G>A MANE Select	NP_001104026.1:p.Gly2408Ser
NM_001456.4:c.7198G>A	NP_001447.2:p.Gly2400Ser