Canonical Allele Identifier: CA415194499

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581268A>T (hg19) ; chrX:g.154352900A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352900A>T , CM000685.2:g.154352900A>T	GRCh38
NC_000023.10:g.153581268A>T , CM000685.1:g.153581268A>T	GRCh37
NC_000023.9:g.153234462A>T	NCBI36
NG_011506.1:g.26739T>A
NG_011506.2:g.26739T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6227T>A	ENSP00000353467.4:p.Ile2076Asn
ENST00000369850.10:c.6251T>A MANE Select	ENSP00000358866.3:p.Ile2084Asn
ENST00000369856.8:c.6170T>A	ENSP00000358872.4:p.Ile2057Asn
ENST00000422373.6:c.3161-225T>A	ENSP00000416926.2:n.3161-225T>A
ENST00000610817.5:c.6308T>A	ENSP00000480593.2:n.6308T>A
ENST00000673639.2:c.280-4210T>A
ENST00000676696.1:c.6530T>A	ENSP00000503392.1:n.6530T>A
ENST00000678304.1:n.1430T>A
ENST00000344736.8:c.6131T>A	ENSP00000358863.3:p.Ile2044Asn
ENST00000360319.8:c.6227T>A	ENSP00000353467.4:p.Ile2076Asn
ENST00000369850.7:c.6251T>A	ENSP00000358866.3:p.Ile2084Asn
ENST00000369856.7:c.6170T>A	ENSP00000358872.4:p.Ile2057Asn
ENST00000415241.1:c.453T>A
ENST00000420627.5:c.6207T>A	ENSP00000408921.1:n.6207T>A
ENST00000422373.5:c.6227T>A	ENSP00000416926.1:p.Ile2076Asn
ENST00000444578.1:c.194T>A	ENSP00000397824.1:p.Ile65Asn
ENST00000466325.1:n.466T>A
ENST00000490936.5:n.2240T>A
ENST00000610817.4:c.5844+493T>A	ENSP00000480593.1:n.5844+493T>A
NM_001110556.1:c.6251T>A	NP_001104026.1:p.Ile2084Asn
NM_001456.3:c.6227T>A	NP_001447.2:p.Ile2076Asn
XM_011531127.1:c.6155T>A	XP_011529429.1:p.Ile2052Asn
XM_011531128.1:c.6131T>A	XP_011529430.1:p.Ile2044Asn
XM_011531129.1:c.6077T>A	XP_011529431.1:p.Ile2026Asn
XM_011531130.1:c.6053T>A	XP_011529432.1:p.Ile2018Asn
XM_011531131.1:c.6050T>A	XP_011529433.1:p.Ile2017Asn
NM_001110556.2:c.6251T>A MANE Select	NP_001104026.1:p.Ile2084Asn
NM_001456.4:c.6227T>A	NP_001447.2:p.Ile2076Asn