Canonical Allele Identifier: CA2579738417

Gene: FLNA

Linked Data

• gnomAD v4: X-154371302-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371302T>G , CM000685.2:g.154371302T>G	GRCh38
NC_000023.10:g.153599670T>G , CM000685.1:g.153599670T>G	GRCh37
NC_000023.9:g.153252864T>G	NCBI36
NG_008677.1:g.1875T>G , LRG_745:g.1875T>G
NG_011506.1:g.8337A>C
NG_011506.2:g.8337A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-57A>C MANE Select	ENSP00000358866.3:n.-57A>C
ENST00000369850.7:c.-57A>C	ENSP00000358866.3:n.-57A>C
ENST00000422373.5:c.-57A>C	ENSP00000416926.1:n.-57A>C
ENST00000610817.4:c.-138A>C	ENSP00000480593.1:n.-138A>C
NM_001110556.1:c.-57A>C	NP_001104026.1:n.-57A>C
NM_001456.3:c.-57A>C	NP_001447.2:n.-57A>C
XM_011531127.1:c.-57A>C	XP_011529429.1:n.-57A>C
XM_011531128.1:c.-57A>C	XP_011529430.1:n.-57A>C
XM_011531129.1:c.-57A>C	XP_011529431.1:n.-57A>C
XM_011531130.1:c.-57A>C	XP_011529432.1:n.-57A>C
XM_011531131.1:c.-57A>C	XP_011529433.1:n.-57A>C
NM_001110556.2:c.-57A>C MANE Select	NP_001104026.1:n.-57A>C
NM_001456.4:c.-57A>C	NP_001447.2:n.-57A>C