Canonical Allele Identifier: CA2824295706

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371267_154371268insAT , CM000685.2:g.154371267_154371268insAT	GRCh38
NC_000023.10:g.153599635_153599636insAT , CM000685.1:g.153599635_153599636insAT	GRCh37
NC_000023.9:g.153252829_153252830insAT	NCBI36
NG_008677.1:g.1840_1841insAT , LRG_745:g.1840_1841insAT
NG_011506.1:g.8371_8372insAT
NG_011506.2:g.8371_8372insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.-23_-22insAT	ENSP00000353467.4:n.-23_-22insAT
ENST00000369850.10:c.-23_-22insAT MANE Select	ENSP00000358866.3:n.-23_-22insAT
ENST00000422373.6:c.-23_-22insAT	ENSP00000416926.2:n.-23_-22insAT
ENST00000344736.8:c.-23_-22insAT	ENSP00000358863.3:n.-23_-22insAT
ENST00000360319.8:c.-23_-22insAT	ENSP00000353467.4:n.-23_-22insAT
ENST00000369850.7:c.-23_-22insAT	ENSP00000358866.3:n.-23_-22insAT
ENST00000422373.5:c.-23_-22insAT	ENSP00000416926.1:n.-23_-22insAT
ENST00000610817.4:c.-104_-103insAT	ENSP00000480593.1:n.-104_-103insAT
NM_001110556.1:c.-23_-22insAT	NP_001104026.1:n.-23_-22insAT
NM_001456.3:c.-23_-22insAT	NP_001447.2:n.-23_-22insAT
XM_011531127.1:c.-23_-22insAT	XP_011529429.1:n.-23_-22insAT
XM_011531128.1:c.-23_-22insAT	XP_011529430.1:n.-23_-22insAT
XM_011531129.1:c.-23_-22insAT	XP_011529431.1:n.-23_-22insAT
XM_011531130.1:c.-23_-22insAT	XP_011529432.1:n.-23_-22insAT
XM_011531131.1:c.-23_-22insAT	XP_011529433.1:n.-23_-22insAT
NM_001110556.2:c.-23_-22insAT MANE Select	NP_001104026.1:n.-23_-22insAT
NM_001456.4:c.-23_-22insAT	NP_001447.2:n.-23_-22insAT