Canonical Allele Identifier: CA2695113852

Gene: FLNA

Linked Data

• gnomAD v4: X-154371286-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371286G>C , CM000685.2:g.154371286G>C	GRCh38
NC_000023.10:g.153599654G>C , CM000685.1:g.153599654G>C	GRCh37
NC_000023.9:g.153252848G>C	NCBI36
NG_008677.1:g.1859G>C , LRG_745:g.1859G>C
NG_011506.1:g.8353C>G
NG_011506.2:g.8353C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-41C>G MANE Select	ENSP00000358866.3:n.-41C>G
ENST00000344736.8:c.-41C>G	ENSP00000358863.3:n.-41C>G
ENST00000369850.7:c.-41C>G	ENSP00000358866.3:n.-41C>G
ENST00000422373.5:c.-41C>G	ENSP00000416926.1:n.-41C>G
ENST00000610817.4:c.-122C>G	ENSP00000480593.1:n.-122C>G
NM_001110556.1:c.-41C>G	NP_001104026.1:n.-41C>G
NM_001456.3:c.-41C>G	NP_001447.2:n.-41C>G
XM_011531127.1:c.-41C>G	XP_011529429.1:n.-41C>G
XM_011531128.1:c.-41C>G	XP_011529430.1:n.-41C>G
XM_011531129.1:c.-41C>G	XP_011529431.1:n.-41C>G
XM_011531130.1:c.-41C>G	XP_011529432.1:n.-41C>G
XM_011531131.1:c.-41C>G	XP_011529433.1:n.-41C>G
NM_001110556.2:c.-41C>G MANE Select	NP_001104026.1:n.-41C>G
NM_001456.4:c.-41C>G	NP_001447.2:n.-41C>G