Canonical Allele Identifier: CA2695113820

Gene: FLNA

Linked Data

• gnomAD v4: X-154371271-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371271_154371272insT , CM000685.2:g.154371271_154371272insT	GRCh38
NC_000023.10:g.153599639_153599640insT , CM000685.1:g.153599639_153599640insT	GRCh37
NC_000023.9:g.153252833_153252834insT	NCBI36
NG_008677.1:g.1844_1845insT , LRG_745:g.1844_1845insT
NG_011506.1:g.8367_8368insA
NG_011506.2:g.8367_8368insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.-27_-26insA	ENSP00000353467.4:n.-27_-26insA
ENST00000369850.10:c.-27_-26insA MANE Select	ENSP00000358866.3:n.-27_-26insA
ENST00000422373.6:c.-27_-26insA	ENSP00000416926.2:n.-27_-26insA
ENST00000344736.8:c.-27_-26insA	ENSP00000358863.3:n.-27_-26insA
ENST00000360319.8:c.-27_-26insA	ENSP00000353467.4:n.-27_-26insA
ENST00000369850.7:c.-27_-26insA	ENSP00000358866.3:n.-27_-26insA
ENST00000422373.5:c.-27_-26insA	ENSP00000416926.1:n.-27_-26insA
ENST00000610817.4:c.-108_-107insA	ENSP00000480593.1:n.-108_-107insA
NM_001110556.1:c.-27_-26insA	NP_001104026.1:n.-27_-26insA
NM_001456.3:c.-27_-26insA	NP_001447.2:n.-27_-26insA
XM_011531127.1:c.-27_-26insA	XP_011529429.1:n.-27_-26insA
XM_011531128.1:c.-27_-26insA	XP_011529430.1:n.-27_-26insA
XM_011531129.1:c.-27_-26insA	XP_011529431.1:n.-27_-26insA
XM_011531130.1:c.-27_-26insA	XP_011529432.1:n.-27_-26insA
XM_011531131.1:c.-27_-26insA	XP_011529433.1:n.-27_-26insA
NM_001110556.2:c.-27_-26insA MANE Select	NP_001104026.1:n.-27_-26insA
NM_001456.4:c.-27_-26insA	NP_001447.2:n.-27_-26insA