Canonical Allele Identifier: CA10560160

Gene: FLNA

Linked Data

• dbSNP Id: rs782337986
• ExAC: X:153581472 C / T
• gnomAD v2: X-153581472-C-T
• MyVariant Identifiers: chrX:g.153581472C>T (hg19) ; chrX:g.154353104C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353104C>T , CM000685.2:g.154353104C>T	GRCh38
NC_000023.10:g.153581472C>T , CM000685.1:g.153581472C>T	GRCh37
NC_000023.9:g.153234666C>T	NCBI36
NG_011506.1:g.26535G>A
NG_011506.2:g.26535G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6099G>A	ENSP00000353467.4:p.Gln2033=
ENST00000369850.10:c.6123G>A MANE Select	ENSP00000358866.3:p.Gln2041=
ENST00000369856.8:c.6042G>A	ENSP00000358872.4:p.Gln2014=
ENST00000422373.6:c.3161-429G>A	ENSP00000416926.2:n.3161-429G>A
ENST00000610817.5:c.6180G>A	ENSP00000480593.2:n.6180G>A
ENST00000673639.2:c.280-4414G>A
ENST00000676696.1:c.6402G>A	ENSP00000503392.1:n.6402G>A
ENST00000678304.1:n.1302G>A
ENST00000344736.8:c.6003G>A	ENSP00000358863.3:p.Gln2001=
ENST00000360319.8:c.6099G>A	ENSP00000353467.4:p.Gln2033=
ENST00000369850.7:c.6123G>A	ENSP00000358866.3:p.Gln2041=
ENST00000369856.7:c.6042G>A	ENSP00000358872.4:p.Gln2014=
ENST00000415241.1:c.325G>A
ENST00000420627.5:c.6079G>A	ENSP00000408921.1:n.6079G>A
ENST00000422373.5:c.6099G>A	ENSP00000416926.1:p.Gln2033=
ENST00000444578.1:c.66G>A	ENSP00000397824.1:p.Gln22=
ENST00000466325.1:n.262G>A
ENST00000490936.5:n.2112G>A
ENST00000610817.4:c.5844+289G>A	ENSP00000480593.1:n.5844+289G>A
NM_001110556.1:c.6123G>A	NP_001104026.1:p.Gln2041=
NM_001456.3:c.6099G>A	NP_001447.2:p.Gln2033=
XM_011531127.1:c.6027G>A	XP_011529429.1:p.Gln2009=
XM_011531128.1:c.6003G>A	XP_011529430.1:p.Gln2001=
XM_011531129.1:c.5949G>A	XP_011529431.1:p.Gln1983=
XM_011531130.1:c.5925G>A	XP_011529432.1:p.Gln1975=
XM_011531131.1:c.5922G>A	XP_011529433.1:p.Gln1974=
NM_001110556.2:c.6123G>A MANE Select	NP_001104026.1:p.Gln2041=
NM_001456.4:c.6099G>A	NP_001447.2:p.Gln2033=