Canonical Allele Identifier: CA2466660587

Gene: FLNA

Linked Data

• dbSNP Id: rs2067807406
• gnomAD v4: X-154371407-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371408dup , CM000685.2:g.154371408dup	GRCh38
NC_000023.10:g.153599776dup , CM000685.1:g.153599776dup	GRCh37
NC_000023.9:g.153252970dup	NCBI36
NG_008677.1:g.1981dup , LRG_745:g.1981dup
NG_011506.1:g.8231dup
NG_011506.2:g.8231dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-116-47dup MANE Select	ENSP00000358866.3:n.-116-47dup
ENST00000369850.7:c.-116-47dup	ENSP00000358866.3:n.-116-47dup
ENST00000422373.5:c.-116-47dup	ENSP00000416926.1:n.-116-47dup
ENST00000610817.4:c.-197-47dup	ENSP00000480593.1:n.-197-47dup
NM_001110556.1:c.-116-47dup	NP_001104026.1:n.-116-47dup
NM_001456.3:c.-116-47dup	NP_001447.2:n.-116-47dup
XM_011531127.1:c.-116-47dup	XP_011529429.1:n.-116-47dup
XM_011531128.1:c.-116-47dup	XP_011529430.1:n.-116-47dup
XM_011531129.1:c.-116-47dup	XP_011529431.1:n.-116-47dup
XM_011531130.1:c.-116-47dup	XP_011529432.1:n.-116-47dup
XM_011531131.1:c.-116-47dup	XP_011529433.1:n.-116-47dup
NM_001110556.2:c.-116-47dup MANE Select	NP_001104026.1:n.-116-47dup
NM_001456.4:c.-116-47dup	NP_001447.2:n.-116-47dup