Canonical Allele Identifier: CA2579738428

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371341A>G , CM000685.2:g.154371341A>G	GRCh38
NC_000023.10:g.153599709A>G , CM000685.1:g.153599709A>G	GRCh37
NC_000023.9:g.153252903A>G	NCBI36
NG_008677.1:g.1914A>G , LRG_745:g.1914A>G
NG_011506.1:g.8298T>C
NG_011506.2:g.8298T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-96T>C MANE Select	ENSP00000358866.3:n.-96T>C
ENST00000369850.7:c.-96T>C	ENSP00000358866.3:n.-96T>C
ENST00000422373.5:c.-96T>C	ENSP00000416926.1:n.-96T>C
ENST00000610817.4:c.-177T>C	ENSP00000480593.1:n.-177T>C
NM_001110556.1:c.-96T>C	NP_001104026.1:n.-96T>C
NM_001456.3:c.-96T>C	NP_001447.2:n.-96T>C
XM_011531127.1:c.-96T>C	XP_011529429.1:n.-96T>C
XM_011531128.1:c.-96T>C	XP_011529430.1:n.-96T>C
XM_011531129.1:c.-96T>C	XP_011529431.1:n.-96T>C
XM_011531130.1:c.-96T>C	XP_011529432.1:n.-96T>C
XM_011531131.1:c.-96T>C	XP_011529433.1:n.-96T>C
NM_001110556.2:c.-96T>C MANE Select	NP_001104026.1:n.-96T>C
NM_001456.4:c.-96T>C	NP_001447.2:n.-96T>C