Canonical Allele Identifier: CA415196476

Gene: FLNA

Linked Data

• dbSNP Id: rs2067635001
• MyVariant Identifiers: chrX:g.153581538G>C (hg19) ; chrX:g.154353170G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353170G>C , CM000685.2:g.154353170G>C	GRCh38
NC_000023.10:g.153581538G>C , CM000685.1:g.153581538G>C	GRCh37
NC_000023.9:g.153234732G>C	NCBI36
NG_011506.1:g.26469C>G
NG_011506.2:g.26469C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6033C>G	ENSP00000353467.4:p.His2011Gln
ENST00000369850.10:c.6057C>G MANE Select	ENSP00000358866.3:p.His2019Gln
ENST00000369856.8:c.5976C>G	ENSP00000358872.4:p.His1992Gln
ENST00000422373.6:c.3161-495C>G	ENSP00000416926.2:n.3161-495C>G
ENST00000610817.5:c.6114C>G	ENSP00000480593.2:n.6114C>G
ENST00000673639.2:c.280-4480C>G
ENST00000676696.1:c.6336C>G	ENSP00000503392.1:n.6336C>G
ENST00000678304.1:n.1236C>G
ENST00000344736.8:c.5937C>G	ENSP00000358863.3:p.His1979Gln
ENST00000360319.8:c.6033C>G	ENSP00000353467.4:p.His2011Gln
ENST00000369850.7:c.6057C>G	ENSP00000358866.3:p.His2019Gln
ENST00000369856.7:c.5976C>G	ENSP00000358872.4:p.His1992Gln
ENST00000415241.1:c.259C>G
ENST00000420627.5:c.6013C>G	ENSP00000408921.1:n.6013C>G
ENST00000422373.5:c.6033C>G	ENSP00000416926.1:p.His2011Gln
ENST00000466325.1:n.196C>G
ENST00000490936.5:n.2046C>G
ENST00000610817.4:c.5844+223C>G	ENSP00000480593.1:n.5844+223C>G
NM_001110556.1:c.6057C>G	NP_001104026.1:p.His2019Gln
NM_001456.3:c.6033C>G	NP_001447.2:p.His2011Gln
XM_011531127.1:c.5961C>G	XP_011529429.1:p.His1987Gln
XM_011531128.1:c.5937C>G	XP_011529430.1:p.His1979Gln
XM_011531129.1:c.5883C>G	XP_011529431.1:p.His1961Gln
XM_011531130.1:c.5859C>G	XP_011529432.1:p.His1953Gln
XM_011531131.1:c.5856C>G	XP_011529433.1:p.His1952Gln
NM_001110556.2:c.6057C>G MANE Select	NP_001104026.1:p.His2019Gln
NM_001456.4:c.6033C>G	NP_001447.2:p.His2011Gln