Canonical Allele Identifier: CA415255698
Community Standard Title: NM_001110556.2(FLNA):c.71G>T (p.Arg24Leu)
Gene: FLNA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154371175C>A , CM000685.2:g.154371175C>A GRCh38
NC_000023.10:g.153599543C>A , CM000685.1:g.153599543C>A GRCh37
NC_000023.9:g.153252737C>A NCBI36
NG_008677.1:g.1748C>A , LRG_745:g.1748C>A
NG_011506.1:g.8464G>T
NG_011506.2:g.8464G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001110556.2:c.71G>T MANE Select NP_001104026.1:p.Arg24Leu
ENST00000369850.10:c.71G>T MANE Select ENSP00000358866.3:p.Arg24Leu
NM_001110556.1:c.71G>T NP_001104026.1:p.Arg24Leu
NM_001456.3:c.71G>T NP_001447.2:p.Arg24Leu
NM_001456.4:c.71G>T NP_001447.2:p.Arg24Leu
ENST00000344736.8:c.71G>T ENSP00000358863.3:p.Arg24Leu
ENST00000360319.8:c.71G>T ENSP00000353467.4:p.Arg24Leu
ENST00000360319.9:c.71G>T ENSP00000353467.4:p.Arg24Leu
ENST00000369850.7:c.71G>T ENSP00000358866.3:p.Arg24Leu
ENST00000369856.7:c.-11G>T ENSP00000358872.4:n.-11G>T
ENST00000369856.8:c.-11G>T ENSP00000358872.4:n.-11G>T
ENST00000420627.5:c.29G>T ENSP00000408921.1:p.Arg10Leu
ENST00000422373.5:c.71G>T ENSP00000416926.1:p.Arg24Leu
ENST00000422373.6:c.71G>T ENSP00000416926.2:p.Arg24Leu
ENST00000610817.4:c.-11G>T ENSP00000480593.1:n.-11G>T
ENST00000610817.5:c.71G>T ENSP00000480593.2:p.Arg24Leu
ENST00000676696.1:c.71G>T ENSP00000503392.1:p.Arg24Leu
XM_011531127.1:c.71G>T XP_011529429.1:p.Arg24Leu
XM_011531128.1:c.71G>T XP_011529430.1:p.Arg24Leu
XM_011531129.1:c.71G>T XP_011529431.1:p.Arg24Leu
XM_011531130.1:c.71G>T XP_011529432.1:p.Arg24Leu
XM_011531131.1:c.71G>T XP_011529433.1:p.Arg24Leu