Canonical Allele Identifier: CA415197536

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581729G>T (hg19) ; chrX:g.154353361G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353361G>T , CM000685.2:g.154353361G>T	GRCh38
NC_000023.10:g.153581729G>T , CM000685.1:g.153581729G>T	GRCh37
NC_000023.9:g.153234923G>T	NCBI36
NG_011506.1:g.26278C>A
NG_011506.2:g.26278C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5933C>A	ENSP00000353467.4:p.Thr1978Asn
ENST00000369850.10:c.5957C>A MANE Select	ENSP00000358866.3:p.Thr1986Asn
ENST00000369856.8:c.5876C>A	ENSP00000358872.4:p.Thr1959Asn
ENST00000422373.6:c.3161-686C>A	ENSP00000416926.2:n.3161-686C>A
ENST00000610817.5:c.6014C>A	ENSP00000480593.2:n.6014C>A
ENST00000673639.2:c.280-4671C>A
ENST00000676696.1:c.6236C>A	ENSP00000503392.1:n.6236C>A
ENST00000678304.1:n.1136C>A
ENST00000344736.8:c.5837C>A	ENSP00000358863.3:p.Thr1946Asn
ENST00000360319.8:c.5933C>A	ENSP00000353467.4:p.Thr1978Asn
ENST00000369850.7:c.5957C>A	ENSP00000358866.3:p.Thr1986Asn
ENST00000369856.7:c.5876C>A	ENSP00000358872.4:p.Thr1959Asn
ENST00000415241.1:c.142C>A
ENST00000420627.5:c.5913C>A	ENSP00000408921.1:n.5913C>A
ENST00000422373.5:c.5933C>A	ENSP00000416926.1:p.Thr1978Asn
ENST00000438732.2:c.631C>A
ENST00000466325.1:n.96C>A
ENST00000490936.5:n.1946C>A
ENST00000610817.4:c.5844+32C>A	ENSP00000480593.1:n.5844+32C>A
NM_001110556.1:c.5957C>A	NP_001104026.1:p.Thr1986Asn
NM_001456.3:c.5933C>A	NP_001447.2:p.Thr1978Asn
XM_011531127.1:c.5861C>A	XP_011529429.1:p.Thr1954Asn
XM_011531128.1:c.5837C>A	XP_011529430.1:p.Thr1946Asn
XM_011531129.1:c.5783C>A	XP_011529431.1:p.Thr1928Asn
XM_011531130.1:c.5759C>A	XP_011529432.1:p.Thr1920Asn
XM_011531131.1:c.5756C>A	XP_011529433.1:p.Thr1919Asn
NM_001110556.2:c.5957C>A MANE Select	NP_001104026.1:p.Thr1986Asn
NM_001456.4:c.5933C>A	NP_001447.2:p.Thr1978Asn