Canonical Allele Identifier: CA2695114183

Gene: FLNA

Linked Data

• gnomAD v4: X-154371408-GAGGGCGGGCCTCCTGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371409_154371424del , CM000685.2:g.154371409_154371424del	GRCh38
NC_000023.10:g.153599777_153599792del , CM000685.1:g.153599777_153599792del	GRCh37
NC_000023.9:g.153252971_153252986del	NCBI36
NG_008677.1:g.1982_1997del , LRG_745:g.1982_1997del
NG_011506.1:g.8215_8230del
NG_011506.2:g.8215_8230del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-116-63_-116-48del MANE Select	ENSP00000358866.3:n.-116-63_-116-48del
ENST00000369850.7:c.-116-63_-116-48del	ENSP00000358866.3:n.-116-63_-116-48del
ENST00000422373.5:c.-116-63_-116-48del	ENSP00000416926.1:n.-116-63_-116-48del
ENST00000610817.4:c.-197-63_-197-48del	ENSP00000480593.1:n.-197-63_-197-48del
NM_001110556.1:c.-116-63_-116-48del	NP_001104026.1:n.-116-63_-116-48del
NM_001456.3:c.-116-63_-116-48del	NP_001447.2:n.-116-63_-116-48del
XM_011531127.1:c.-116-63_-116-48del	XP_011529429.1:n.-116-63_-116-48del
XM_011531128.1:c.-116-63_-116-48del	XP_011529430.1:n.-116-63_-116-48del
XM_011531129.1:c.-116-63_-116-48del	XP_011529431.1:n.-116-63_-116-48del
XM_011531130.1:c.-116-63_-116-48del	XP_011529432.1:n.-116-63_-116-48del
XM_011531131.1:c.-116-63_-116-48del	XP_011529433.1:n.-116-63_-116-48del
NM_001110556.2:c.-116-63_-116-48del MANE Select	NP_001104026.1:n.-116-63_-116-48del
NM_001456.4:c.-116-63_-116-48del	NP_001447.2:n.-116-63_-116-48del