Canonical Allele Identifier: CA2824295729

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371466_154371467dup , CM000685.2:g.154371466_154371467dup	GRCh38
NC_000023.10:g.153599834_153599835dup , CM000685.1:g.153599834_153599835dup	GRCh37
NC_000023.9:g.153253028_153253029dup	NCBI36
NG_008677.1:g.2039_2040dup , LRG_745:g.2039_2040dup
NG_011506.1:g.8174_8175dup
NG_011506.2:g.8174_8175dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-116-104_-116-103dup MANE Select	ENSP00000358866.3:n.-116-104_-116-103dup
ENST00000369850.7:c.-116-104_-116-103dup	ENSP00000358866.3:n.-116-104_-116-103dup
ENST00000422373.5:c.-116-104_-116-103dup	ENSP00000416926.1:n.-116-104_-116-103dup
ENST00000610817.4:c.-197-104_-197-103dup	ENSP00000480593.1:n.-197-104_-197-103dup
NM_001110556.1:c.-116-104_-116-103dup	NP_001104026.1:n.-116-104_-116-103dup
NM_001456.3:c.-116-104_-116-103dup	NP_001447.2:n.-116-104_-116-103dup
XM_011531127.1:c.-116-104_-116-103dup	XP_011529429.1:n.-116-104_-116-103dup
XM_011531128.1:c.-116-104_-116-103dup	XP_011529430.1:n.-116-104_-116-103dup
XM_011531129.1:c.-116-104_-116-103dup	XP_011529431.1:n.-116-104_-116-103dup
XM_011531130.1:c.-116-104_-116-103dup	XP_011529432.1:n.-116-104_-116-103dup
XM_011531131.1:c.-116-104_-116-103dup	XP_011529433.1:n.-116-104_-116-103dup
NM_001110556.2:c.-116-104_-116-103dup MANE Select	NP_001104026.1:n.-116-104_-116-103dup
NM_001456.4:c.-116-104_-116-103dup	NP_001447.2:n.-116-104_-116-103dup