Canonical Allele Identifier: CA415192874

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581138A>C (hg19) ; chrX:g.154352770A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352770A>C , CM000685.2:g.154352770A>C	GRCh38
NC_000023.10:g.153581138A>C , CM000685.1:g.153581138A>C	GRCh37
NC_000023.9:g.153234332A>C	NCBI36
NG_011506.1:g.26869T>G
NG_011506.2:g.26869T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6355+2T>G	ENSP00000353467.4:n.6355+2T>G
ENST00000369850.10:c.6379+2T>G MANE Select	ENSP00000358866.3:n.6379+2T>G
ENST00000369856.8:c.6298+2T>G	ENSP00000358872.4:n.6298+2T>G
ENST00000422373.6:c.3161-95T>G	ENSP00000416926.2:n.3161-95T>G
ENST00000610817.5:c.6436+2T>G	ENSP00000480593.2:n.6436+2T>G
ENST00000673639.2:c.280-4080T>G
ENST00000676696.1:c.6658+2T>G	ENSP00000503392.1:n.6658+2T>G
ENST00000678304.1:n.1558+2T>G
ENST00000344736.8:c.6259+2T>G	ENSP00000358863.3:n.6259+2T>G
ENST00000360319.8:c.6355+2T>G	ENSP00000353467.4:n.6355+2T>G
ENST00000369850.7:c.6379+2T>G	ENSP00000358866.3:n.6379+2T>G
ENST00000369856.7:c.6298+2T>G	ENSP00000358872.4:n.6298+2T>G
ENST00000415241.1:c.581+2T>G
ENST00000420627.5:c.6335+2T>G	ENSP00000408921.1:n.6335+2T>G
ENST00000422373.5:c.6355+2T>G	ENSP00000416926.1:n.6355+2T>G
ENST00000444578.1:c.322+2T>G	ENSP00000397824.1:n.322+2T>G
ENST00000466325.1:n.596T>G
ENST00000474358.5:n.12+2T>G
ENST00000490936.5:n.2368+2T>G
ENST00000498411.1:n.67+47T>G
ENST00000610817.4:c.5844+623T>G	ENSP00000480593.1:n.5844+623T>G
NM_001110556.1:c.6379+2T>G	NP_001104026.1:n.6379+2T>G
NM_001456.3:c.6355+2T>G	NP_001447.2:n.6355+2T>G
XM_011531127.1:c.6283+2T>G	XP_011529429.1:n.6283+2T>G
XM_011531128.1:c.6259+2T>G	XP_011529430.1:n.6259+2T>G
XM_011531129.1:c.6205+2T>G	XP_011529431.1:n.6205+2T>G
XM_011531130.1:c.6181+2T>G	XP_011529432.1:n.6181+2T>G
XM_011531131.1:c.6178+2T>G	XP_011529433.1:n.6178+2T>G
NM_001110556.2:c.6379+2T>G MANE Select	NP_001104026.1:n.6379+2T>G
NM_001456.4:c.6355+2T>G	NP_001447.2:n.6355+2T>G