Canonical Allele Identifier: CA415195449

Gene: FLNA

Linked Data

• MyVariant Identifiers: chrX:g.153581414G>C (hg19) ; chrX:g.154353046G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353046G>C , CM000685.2:g.154353046G>C	GRCh38
NC_000023.10:g.153581414G>C , CM000685.1:g.153581414G>C	GRCh37
NC_000023.9:g.153234608G>C	NCBI36
NG_011506.1:g.26593C>G
NG_011506.2:g.26593C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6157C>G	ENSP00000353467.4:p.His2053Asp
ENST00000369850.10:c.6181C>G MANE Select	ENSP00000358866.3:p.His2061Asp
ENST00000369856.8:c.6100C>G	ENSP00000358872.4:p.His2034Asp
ENST00000422373.6:c.3161-371C>G	ENSP00000416926.2:n.3161-371C>G
ENST00000610817.5:c.6238C>G	ENSP00000480593.2:n.6238C>G
ENST00000673639.2:c.280-4356C>G
ENST00000676696.1:c.6460C>G	ENSP00000503392.1:n.6460C>G
ENST00000678304.1:n.1360C>G
ENST00000344736.8:c.6061C>G	ENSP00000358863.3:p.His2021Asp
ENST00000360319.8:c.6157C>G	ENSP00000353467.4:p.His2053Asp
ENST00000369850.7:c.6181C>G	ENSP00000358866.3:p.His2061Asp
ENST00000369856.7:c.6100C>G	ENSP00000358872.4:p.His2034Asp
ENST00000415241.1:c.383C>G
ENST00000420627.5:c.6137C>G	ENSP00000408921.1:n.6137C>G
ENST00000422373.5:c.6157C>G	ENSP00000416926.1:p.His2053Asp
ENST00000444578.1:c.124C>G	ENSP00000397824.1:p.His42Asp
ENST00000466325.1:n.320C>G
ENST00000490936.5:n.2170C>G
ENST00000610817.4:c.5844+347C>G	ENSP00000480593.1:n.5844+347C>G
NM_001110556.1:c.6181C>G	NP_001104026.1:p.His2061Asp
NM_001456.3:c.6157C>G	NP_001447.2:p.His2053Asp
XM_011531127.1:c.6085C>G	XP_011529429.1:p.His2029Asp
XM_011531128.1:c.6061C>G	XP_011529430.1:p.His2021Asp
XM_011531129.1:c.6007C>G	XP_011529431.1:p.His2003Asp
XM_011531130.1:c.5983C>G	XP_011529432.1:p.His1995Asp
XM_011531131.1:c.5980C>G	XP_011529433.1:p.His1994Asp
NM_001110556.2:c.6181C>G MANE Select	NP_001104026.1:p.His2061Asp
NM_001456.4:c.6157C>G	NP_001447.2:p.His2053Asp