Canonical Allele Identifier: CA2824295707

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371324_154371325insC , CM000685.2:g.154371324_154371325insC	GRCh38
NC_000023.10:g.153599692_153599693insC , CM000685.1:g.153599692_153599693insC	GRCh37
NC_000023.9:g.153252886_153252887insC	NCBI36
NG_008677.1:g.1897_1898insC , LRG_745:g.1897_1898insC
NG_011506.1:g.8314_8315insG
NG_011506.2:g.8314_8315insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-80_-79insG MANE Select	ENSP00000358866.3:n.-80_-79insG
ENST00000369850.7:c.-80_-79insG	ENSP00000358866.3:n.-80_-79insG
ENST00000422373.5:c.-80_-79insG	ENSP00000416926.1:n.-80_-79insG
ENST00000610817.4:c.-161_-160insG	ENSP00000480593.1:n.-161_-160insG
NM_001110556.1:c.-80_-79insG	NP_001104026.1:n.-80_-79insG
NM_001456.3:c.-80_-79insG	NP_001447.2:n.-80_-79insG
XM_011531127.1:c.-80_-79insG	XP_011529429.1:n.-80_-79insG
XM_011531128.1:c.-80_-79insG	XP_011529430.1:n.-80_-79insG
XM_011531129.1:c.-80_-79insG	XP_011529431.1:n.-80_-79insG
XM_011531130.1:c.-80_-79insG	XP_011529432.1:n.-80_-79insG
XM_011531131.1:c.-80_-79insG	XP_011529433.1:n.-80_-79insG
NM_001110556.2:c.-80_-79insG MANE Select	NP_001104026.1:n.-80_-79insG
NM_001456.4:c.-80_-79insG	NP_001447.2:n.-80_-79insG