Canonical Allele Identifier: CA415214762

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153586629G>T (hg19) ; chrX:g.154358261G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154358261G>T , CM000685.2:g.154358261G>T	GRCh38
NC_000023.10:g.153586629G>T , CM000685.1:g.153586629G>T	GRCh37
NC_000023.9:g.153239823G>T	NCBI36
NG_011506.1:g.21378C>A
NG_011506.2:g.21378C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.4693C>A	ENSP00000353467.4:p.Pro1565Thr
ENST00000369850.10:c.4693C>A MANE Select	ENSP00000358866.3:p.Pro1565Thr
ENST00000369856.8:c.4612C>A	ENSP00000358872.4:p.Pro1538Thr
ENST00000422373.6:c.3160+3094C>A	ENSP00000416926.2:n.3160+3094C>A
ENST00000610817.5:c.4750C>A	ENSP00000480593.2:n.4750C>A
ENST00000673639.2:c.279+7175C>A
ENST00000676696.1:c.4972C>A	ENSP00000503392.1:n.4972C>A
ENST00000678304.1:n.148+828C>A
ENST00000344736.8:c.4693C>A	ENSP00000358863.3:p.Pro1565Thr
ENST00000360319.8:c.4693C>A	ENSP00000353467.4:p.Pro1565Thr
ENST00000369850.7:c.4693C>A	ENSP00000358866.3:p.Pro1565Thr
ENST00000369856.7:c.4612C>A	ENSP00000358872.4:p.Pro1538Thr
ENST00000420627.5:c.4649C>A	ENSP00000408921.1:n.4649C>A
ENST00000422373.5:c.4693C>A	ENSP00000416926.1:p.Pro1565Thr
ENST00000466319.1:n.315C>A
ENST00000490936.5:n.706C>A
ENST00000610817.4:c.4612C>A	ENSP00000480593.1:p.Pro1538Thr
NM_001110556.1:c.4693C>A	NP_001104026.1:p.Pro1565Thr
NM_001456.3:c.4693C>A	NP_001447.2:p.Pro1565Thr
XM_011531127.1:c.4693C>A	XP_011529429.1:p.Pro1565Thr
XM_011531128.1:c.4693C>A	XP_011529430.1:p.Pro1565Thr
XM_011531129.1:c.4693C>A	XP_011529431.1:p.Pro1565Thr
XM_011531130.1:c.4693C>A	XP_011529432.1:p.Pro1565Thr
XM_011531131.1:c.4492C>A	XP_011529433.1:p.Pro1498Thr
NM_001110556.2:c.4693C>A MANE Select	NP_001104026.1:p.Pro1565Thr
NM_001456.4:c.4693C>A	NP_001447.2:p.Pro1565Thr