Canonical Allele Identifier: CA2466660582

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371400C= , CM000685.2:g.154371400C=	GRCh38
NC_000023.10:g.153599768C= , CM000685.1:g.153599768C=	GRCh37
NC_000023.9:g.153252962C=	NCBI36
NG_008677.1:g.1973C= , LRG_745:g.1973C=
NG_011506.1:g.8239G=
NG_011506.2:g.8239G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369850.10:c.-116-39G= MANE Select	ENSP00000358866.3:n.-116-39G=
ENST00000369850.7:c.-116-39G=	ENSP00000358866.3:n.-116-39G=
ENST00000422373.5:c.-116-39G=	ENSP00000416926.1:n.-116-39G=
ENST00000610817.4:c.-197-39G=	ENSP00000480593.1:n.-197-39G=
NM_001110556.1:c.-116-39G=	NP_001104026.1:n.-116-39G=
NM_001456.3:c.-116-39G=	NP_001447.2:n.-116-39G=
XM_011531127.1:c.-116-39G=	XP_011529429.1:n.-116-39G=
XM_011531128.1:c.-116-39G=	XP_011529430.1:n.-116-39G=
XM_011531129.1:c.-116-39G=	XP_011529431.1:n.-116-39G=
XM_011531130.1:c.-116-39G=	XP_011529432.1:n.-116-39G=
XM_011531131.1:c.-116-39G=	XP_011529433.1:n.-116-39G=
NM_001110556.2:c.-116-39G= MANE Select	NP_001104026.1:n.-116-39G=
NM_001456.4:c.-116-39G=	NP_001447.2:n.-116-39G=