Canonical Allele Identifier: CA873335119

Gene: FLNA

Linked Data

• dbSNP Id: rs368240378
• gnomAD v3: X-154350556-C-T
• gnomAD v4: X-154350556-C-T
• MyVariant Identifiers: chrX:g.153578924C>T (hg19) ; chrX:g.154350556C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154350556C>T , CM000685.2:g.154350556C>T	GRCh38
NC_000023.10:g.153578924C>T , CM000685.1:g.153578924C>T	GRCh37
NC_000023.9:g.153232118C>T	NCBI36
NG_011506.1:g.29083G>A
NG_011506.2:g.29083G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.7133-349G>A	ENSP00000353467.4:n.7133-349G>A
ENST00000369850.10:c.7157-349G>A MANE Select	ENSP00000358866.3:n.7157-349G>A
ENST00000369856.8:c.7076-349G>A	ENSP00000358872.4:n.7076-349G>A
ENST00000422373.6:c.3938-349G>A	ENSP00000416926.2:n.3938-349G>A
ENST00000610817.5:c.7214-349G>A	ENSP00000480593.2:n.7214-349G>A
ENST00000673639.2:c.280-1866G>A
ENST00000676696.1:c.7436-349G>A	ENSP00000503392.1:n.7436-349G>A
ENST00000678304.1:n.2875-349G>A
ENST00000344736.8:c.7037-349G>A	ENSP00000358863.3:n.7037-349G>A
ENST00000360319.8:c.7133-349G>A	ENSP00000353467.4:n.7133-349G>A
ENST00000369850.7:c.7157-349G>A	ENSP00000358866.3:n.7157-349G>A
ENST00000369856.7:c.7076-349G>A	ENSP00000358872.4:n.7076-349G>A
ENST00000420627.5:c.7113-349G>A	ENSP00000408921.1:n.7113-349G>A
ENST00000422373.5:c.7133-349G>A	ENSP00000416926.1:n.7133-349G>A
ENST00000490936.5:n.4037G>A
ENST00000498411.1:n.68-1726G>A
ENST00000498491.5:n.198-349G>A
ENST00000610817.4:c.6161-349G>A	ENSP00000480593.1:n.6161-349G>A
NM_001110556.1:c.7157-349G>A	NP_001104026.1:n.7157-349G>A
NM_001456.3:c.7133-349G>A	NP_001447.2:n.7133-349G>A
XM_011531127.1:c.7061-349G>A	XP_011529429.1:n.7061-349G>A
XM_011531128.1:c.7037-349G>A	XP_011529430.1:n.7037-349G>A
XM_011531129.1:c.6983-349G>A	XP_011529431.1:n.6983-349G>A
XM_011531130.1:c.6959-349G>A	XP_011529432.1:n.6959-349G>A
XM_011531131.1:c.6956-349G>A	XP_011529433.1:n.6956-349G>A
NM_001110556.2:c.7157-349G>A MANE Select	NP_001104026.1:n.7157-349G>A
NM_001456.4:c.7133-349G>A	NP_001447.2:n.7133-349G>A