Canonical Allele Identifier: CA2466658998
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154367749_154367758delinsAGGGAGGCTG , CM000685.2:g.154367749_154367758delinsAGGGAGGCTG GRCh38
NC_000023.10:g.153596117_153596126delinsAGGGAGGCTG , CM000685.1:g.153596117_153596126delinsAGGGAGGCTG GRCh37
NC_000023.9:g.153249311_153249320delinsAGGGAGGCTG NCBI36
NG_011506.1:g.11881_11890delinsCAGCCTCCCT
NG_011506.2:g.11881_11890delinsCAGCCTCCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360319.9:c.623-20_623-11delinsCAGCCTCCCT ENSP00000353467.4:n.623-20_623-11delinsCAGCCTCCCT
ENST00000369850.10:c.623-20_623-11delinsCAGCCTCCCT MANE Select ENSP00000358866.3:n.623-20_623-11delinsCAGCCTCCCT
ENST00000369856.8:c.542-20_542-11delinsCAGCCTCCCT ENSP00000358872.4:n.542-20_542-11delinsCAGCCTCCCT
ENST00000422373.6:c.623-20_623-11delinsCAGCCTCCCT ENSP00000416926.2:n.623-20_623-11delinsCAGCCTCCCT
ENST00000610817.5:c.623-20_623-11delinsCAGCCTCCCT ENSP00000480593.2:n.623-20_623-11delinsCAGCCTCCCT
ENST00000676696.1:c.623-20_623-11delinsCAGCCTCCCT ENSP00000503392.1:n.623-20_623-11delinsCAGCCTCCCT
ENST00000344736.8:c.623-20_623-11delinsCAGCCTCCCT ENSP00000358863.3:n.623-20_623-11delinsCAGCCTCCCT
ENST00000360319.8:c.623-20_623-11delinsCAGCCTCCCT ENSP00000353467.4:n.623-20_623-11delinsCAGCCTCCCT
ENST00000369850.7:c.623-20_623-11delinsCAGCCTCCCT ENSP00000358866.3:n.623-20_623-11delinsCAGCCTCCCT
ENST00000369856.7:c.542-20_542-11delinsCAGCCTCCCT ENSP00000358872.4:n.542-20_542-11delinsCAGCCTCCCT
ENST00000420627.5:c.581-20_581-11delinsCAGCCTCCCT ENSP00000408921.1:n.581-20_581-11delinsCAGCCTCCCT
ENST00000422373.5:c.623-20_623-11delinsCAGCCTCCCT ENSP00000416926.1:n.623-20_623-11delinsCAGCCTCCCT
ENST00000610817.4:c.542-20_542-11delinsCAGCCTCCCT ENSP00000480593.1:n.542-20_542-11delinsCAGCCTCCCT
NM_001110556.1:c.623-20_623-11delinsCAGCCTCCCT NP_001104026.1:n.623-20_623-11delinsCAGCCTCCCT
NM_001456.3:c.623-20_623-11delinsCAGCCTCCCT NP_001447.2:n.623-20_623-11delinsCAGCCTCCCT
XM_011531127.1:c.623-20_623-11delinsCAGCCTCCCT XP_011529429.1:n.623-20_623-11delinsCAGCCTCCCT
XM_011531128.1:c.623-20_623-11delinsCAGCCTCCCT XP_011529430.1:n.623-20_623-11delinsCAGCCTCCCT
XM_011531129.1:c.623-20_623-11delinsCAGCCTCCCT XP_011529431.1:n.623-20_623-11delinsCAGCCTCCCT
XM_011531130.1:c.623-20_623-11delinsCAGCCTCCCT XP_011529432.1:n.623-20_623-11delinsCAGCCTCCCT
XM_011531131.1:c.623-20_623-11delinsCAGCCTCCCT XP_011529433.1:n.623-20_623-11delinsCAGCCTCCCT
NM_001110556.2:c.623-20_623-11delinsCAGCCTCCCT MANE Select NP_001104026.1:n.623-20_623-11delinsCAGCCTCCCT
NM_001456.4:c.623-20_623-11delinsCAGCCTCCCT NP_001447.2:n.623-20_623-11delinsCAGCCTCCCT