Canonical Allele Identifier: CA2695113996

Gene: FLNA

Linked Data

• gnomAD v4: X-154371353-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371353G>A , CM000685.2:g.154371353G>A	GRCh38
NC_000023.10:g.153599721G>A , CM000685.1:g.153599721G>A	GRCh37
NC_000023.9:g.153252915G>A	NCBI36
NG_008677.1:g.1926G>A , LRG_745:g.1926G>A
NG_011506.1:g.8286C>T
NG_011506.2:g.8286C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-108C>T MANE Select	ENSP00000358866.3:n.-108C>T
ENST00000369850.7:c.-108C>T	ENSP00000358866.3:n.-108C>T
ENST00000422373.5:c.-108C>T	ENSP00000416926.1:n.-108C>T
ENST00000610817.4:c.-189C>T	ENSP00000480593.1:n.-189C>T
NM_001110556.1:c.-108C>T	NP_001104026.1:n.-108C>T
NM_001456.3:c.-108C>T	NP_001447.2:n.-108C>T
XM_011531127.1:c.-108C>T	XP_011529429.1:n.-108C>T
XM_011531128.1:c.-108C>T	XP_011529430.1:n.-108C>T
XM_011531129.1:c.-108C>T	XP_011529431.1:n.-108C>T
XM_011531130.1:c.-108C>T	XP_011529432.1:n.-108C>T
XM_011531131.1:c.-108C>T	XP_011529433.1:n.-108C>T
NM_001110556.2:c.-108C>T MANE Select	NP_001104026.1:n.-108C>T
NM_001456.4:c.-108C>T	NP_001447.2:n.-108C>T