Canonical Allele Identifier: CA2466660392

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371084G= , CM000685.2:g.154371084G=	GRCh38
NC_000023.10:g.153599452G= , CM000685.1:g.153599452G=	GRCh37
NC_000023.9:g.153252646G=	NCBI36
NG_008677.1:g.1657G= , LRG_745:g.1657G=
NG_011506.1:g.8555C=
NG_011506.2:g.8555C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.162C=	ENSP00000353467.4:p.Asn54=
ENST00000369850.10:c.162C= MANE Select	ENSP00000358866.3:p.Asn54=
ENST00000369856.8:c.81C=	ENSP00000358872.4:p.Asn27=
ENST00000422373.6:c.162C=	ENSP00000416926.2:p.Asn54=
ENST00000610817.5:c.162C=	ENSP00000480593.2:p.Asn54=
ENST00000676696.1:c.162C=	ENSP00000503392.1:p.Asn54=
ENST00000344736.8:c.162C=	ENSP00000358863.3:p.Asn54=
ENST00000360319.8:c.162C=	ENSP00000353467.4:p.Asn54=
ENST00000369850.7:c.162C=	ENSP00000358866.3:p.Asn54=
ENST00000369856.7:c.81C=	ENSP00000358872.4:p.Asn27=
ENST00000420627.5:c.120C=	ENSP00000408921.1:p.Asn40=
ENST00000422373.5:c.162C=	ENSP00000416926.1:p.Asn54=
ENST00000610817.4:c.81C=	ENSP00000480593.1:p.Asn27=
NM_001110556.1:c.162C=	NP_001104026.1:p.Asn54=
NM_001456.3:c.162C=	NP_001447.2:p.Asn54=
XM_011531127.1:c.162C=	XP_011529429.1:p.Asn54=
XM_011531128.1:c.162C=	XP_011529430.1:p.Asn54=
XM_011531129.1:c.162C=	XP_011529431.1:p.Asn54=
XM_011531130.1:c.162C=	XP_011529432.1:p.Asn54=
XM_011531131.1:c.162C=	XP_011529433.1:p.Asn54=
NM_001110556.2:c.162C= MANE Select	NP_001104026.1:p.Asn54=
NM_001456.4:c.162C=	NP_001447.2:p.Asn54=