Canonical Allele Identifier: CA2695114055

Gene: FLNA

Linked Data

• gnomAD v4: X-154371370-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371370A>C , CM000685.2:g.154371370A>C	GRCh38
NC_000023.10:g.153599738A>C , CM000685.1:g.153599738A>C	GRCh37
NC_000023.9:g.153252932A>C	NCBI36
NG_008677.1:g.1943A>C , LRG_745:g.1943A>C
NG_011506.1:g.8269T>G
NG_011506.2:g.8269T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-116-9T>G MANE Select	ENSP00000358866.3:n.-116-9T>G
ENST00000369850.7:c.-116-9T>G	ENSP00000358866.3:n.-116-9T>G
ENST00000422373.5:c.-116-9T>G	ENSP00000416926.1:n.-116-9T>G
ENST00000610817.4:c.-197-9T>G	ENSP00000480593.1:n.-197-9T>G
NM_001110556.1:c.-116-9T>G	NP_001104026.1:n.-116-9T>G
NM_001456.3:c.-116-9T>G	NP_001447.2:n.-116-9T>G
XM_011531127.1:c.-116-9T>G	XP_011529429.1:n.-116-9T>G
XM_011531128.1:c.-116-9T>G	XP_011529430.1:n.-116-9T>G
XM_011531129.1:c.-116-9T>G	XP_011529431.1:n.-116-9T>G
XM_011531130.1:c.-116-9T>G	XP_011529432.1:n.-116-9T>G
XM_011531131.1:c.-116-9T>G	XP_011529433.1:n.-116-9T>G
NM_001110556.2:c.-116-9T>G MANE Select	NP_001104026.1:n.-116-9T>G
NM_001456.4:c.-116-9T>G	NP_001447.2:n.-116-9T>G