Canonical Allele Identifier: CA2695111956

Gene: FLNA

Linked Data

• gnomAD v4: X-154352801-TTGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352807_154352809del , CM000685.2:g.154352807_154352809del	GRCh38
NC_000023.10:g.153581175_153581177del , CM000685.1:g.153581175_153581177del	GRCh37
NC_000023.9:g.153234369_153234371del	NCBI36
NG_011506.1:g.26835_26837del
NG_011506.2:g.26835_26837del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.6323_6325del	ENSP00000353467.4:p.Ile2108del
ENST00000369850.10:c.6347_6349del MANE Select	ENSP00000358866.3:p.Ile2116del
ENST00000369856.8:c.6266_6268del	ENSP00000358872.4:p.Ile2089del
ENST00000422373.6:c.3161-129_3161-127del	ENSP00000416926.2:n.3161-129_3161-127del
ENST00000610817.5:c.6404_6406del	ENSP00000480593.2:n.6404_6406del
ENST00000673639.2:c.280-4114_280-4112del
ENST00000676696.1:c.6626_6628del	ENSP00000503392.1:n.6626_6628del
ENST00000678304.1:n.1526_1528del
ENST00000344736.8:c.6227_6229del	ENSP00000358863.3:p.Ile2076del
ENST00000360319.8:c.6323_6325del	ENSP00000353467.4:p.Ile2108del
ENST00000369850.7:c.6347_6349del	ENSP00000358866.3:p.Ile2116del
ENST00000369856.7:c.6266_6268del	ENSP00000358872.4:p.Ile2089del
ENST00000415241.1:c.549_551del
ENST00000420627.5:c.6303_6305del	ENSP00000408921.1:n.6303_6305del
ENST00000422373.5:c.6323_6325del	ENSP00000416926.1:p.Ile2108del
ENST00000444578.1:c.290_292del	ENSP00000397824.1:p.Ile97del
ENST00000466325.1:n.562_564del
ENST00000490936.5:n.2336_2338del
ENST00000498411.1:n.67+13_67+15del
ENST00000610817.4:c.5844+589_5844+591del	ENSP00000480593.1:n.5844+589_5844+591del
NM_001110556.1:c.6347_6349del	NP_001104026.1:p.Ile2116del
NM_001456.3:c.6323_6325del	NP_001447.2:p.Ile2108del
XM_011531127.1:c.6251_6253del	XP_011529429.1:p.Ile2084del
XM_011531128.1:c.6227_6229del	XP_011529430.1:p.Ile2076del
XM_011531129.1:c.6173_6175del	XP_011529431.1:p.Ile2058del
XM_011531130.1:c.6149_6151del	XP_011529432.1:p.Ile2050del
XM_011531131.1:c.6146_6148del	XP_011529433.1:p.Ile2049del
NM_001110556.2:c.6347_6349del MANE Select	NP_001104026.1:p.Ile2116del
NM_001456.4:c.6323_6325del	NP_001447.2:p.Ile2108del