Canonical Allele Identifier: CA2695113855

Gene: FLNA

Linked Data

• gnomAD v4: X-154371287-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371287G>T , CM000685.2:g.154371287G>T	GRCh38
NC_000023.10:g.153599655G>T , CM000685.1:g.153599655G>T	GRCh37
NC_000023.9:g.153252849G>T	NCBI36
NG_008677.1:g.1860G>T , LRG_745:g.1860G>T
NG_011506.1:g.8352C>A
NG_011506.2:g.8352C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-42C>A MANE Select	ENSP00000358866.3:n.-42C>A
ENST00000344736.8:c.-42C>A	ENSP00000358863.3:n.-42C>A
ENST00000369850.7:c.-42C>A	ENSP00000358866.3:n.-42C>A
ENST00000422373.5:c.-42C>A	ENSP00000416926.1:n.-42C>A
ENST00000610817.4:c.-123C>A	ENSP00000480593.1:n.-123C>A
NM_001110556.1:c.-42C>A	NP_001104026.1:n.-42C>A
NM_001456.3:c.-42C>A	NP_001447.2:n.-42C>A
XM_011531127.1:c.-42C>A	XP_011529429.1:n.-42C>A
XM_011531128.1:c.-42C>A	XP_011529430.1:n.-42C>A
XM_011531129.1:c.-42C>A	XP_011529431.1:n.-42C>A
XM_011531130.1:c.-42C>A	XP_011529432.1:n.-42C>A
XM_011531131.1:c.-42C>A	XP_011529433.1:n.-42C>A
NM_001110556.2:c.-42C>A MANE Select	NP_001104026.1:n.-42C>A
NM_001456.4:c.-42C>A	NP_001447.2:n.-42C>A