Canonical Allele Identifier: CA415184660

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153579279T>G (hg19) ; chrX:g.154350911T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350911T>G , CM000685.2:g.154350911T>G	GRCh38
NC_000023.10:g.153579279T>G , CM000685.1:g.153579279T>G	GRCh37
NC_000023.9:g.153232473T>G	NCBI36
NG_011506.1:g.28728A>C
NG_011506.2:g.28728A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7130A>C	ENSP00000353467.4:p.Gln2377Pro
ENST00000369850.10:c.7154A>C MANE Select	ENSP00000358866.3:p.Gln2385Pro
ENST00000369856.8:c.7073A>C	ENSP00000358872.4:p.Gln2358Pro
ENST00000422373.6:c.3935A>C	ENSP00000416926.2:p.Gln1312Pro
ENST00000610817.5:c.7211A>C	ENSP00000480593.2:n.7211A>C
ENST00000673639.2:c.280-2221A>C
ENST00000676696.1:c.7433A>C	ENSP00000503392.1:n.7433A>C
ENST00000678304.1:n.2872A>C
ENST00000344736.8:c.7034A>C	ENSP00000358863.3:p.Gln2345Pro
ENST00000360319.8:c.7130A>C	ENSP00000353467.4:p.Gln2377Pro
ENST00000369850.7:c.7154A>C	ENSP00000358866.3:p.Gln2385Pro
ENST00000369856.7:c.7073A>C	ENSP00000358872.4:p.Gln2358Pro
ENST00000420627.5:c.7110A>C	ENSP00000408921.1:n.7110A>C
ENST00000422373.5:c.7130A>C	ENSP00000416926.1:p.Gln2377Pro
ENST00000490936.5:n.3682A>C
ENST00000498411.1:n.67+1906A>C
ENST00000498491.5:n.195A>C
ENST00000610817.4:c.6158A>C	ENSP00000480593.1:p.Gln2053Pro
NM_001110556.1:c.7154A>C	NP_001104026.1:p.Gln2385Pro
NM_001456.3:c.7130A>C	NP_001447.2:p.Gln2377Pro
XM_011531127.1:c.7058A>C	XP_011529429.1:p.Gln2353Pro
XM_011531128.1:c.7034A>C	XP_011529430.1:p.Gln2345Pro
XM_011531129.1:c.6980A>C	XP_011529431.1:p.Gln2327Pro
XM_011531130.1:c.6956A>C	XP_011529432.1:p.Gln2319Pro
XM_011531131.1:c.6953A>C	XP_011529433.1:p.Gln2318Pro
NM_001110556.2:c.7154A>C MANE Select	NP_001104026.1:p.Gln2385Pro
NM_001456.4:c.7130A>C	NP_001447.2:p.Gln2377Pro