Canonical Allele Identifier: CA256057

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154360319T>G , CM000685.2:g.154360319T>G	GRCh38
NC_000023.10:g.153588687T>G , CM000685.1:g.153588687T>G	GRCh37
NC_000023.9:g.153241881T>G	NCBI36
NG_011506.1:g.19320A>C
NG_011506.2:g.19320A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001110556.2:c.3476A>C MANE Select	NP_001104026.1:p.Asp1159Ala
ENST00000369850.10:c.3476A>C MANE Select	ENSP00000358866.3:p.Asp1159Ala
NM_001110556.1:c.3476A>C	NP_001104026.1:p.Asp1159Ala
NM_001456.3:c.3476A>C	NP_001447.2:p.Asp1159Ala
NM_001456.4:c.3476A>C	NP_001447.2:p.Asp1159Ala
ENST00000344736.8:c.3476A>C	ENSP00000358863.3:p.Asp1159Ala
ENST00000360319.8:c.3476A>C	ENSP00000353467.4:p.Asp1159Ala
ENST00000360319.9:c.3476A>C	ENSP00000353467.4:p.Asp1159Ala
ENST00000369850.7:c.3476A>C	ENSP00000358866.3:p.Asp1159Ala
ENST00000369856.7:c.3395A>C	ENSP00000358872.4:p.Asp1132Ala
ENST00000369856.8:c.3395A>C	ENSP00000358872.4:p.Asp1132Ala
ENST00000420627.5:c.3432A>C	ENSP00000408921.1:n.3432A>C
ENST00000422373.5:c.3476A>C	ENSP00000416926.1:p.Asp1159Ala
ENST00000422373.6:c.3160+1036A>C	ENSP00000416926.2:n.3160+1036A>C
ENST00000610817.4:c.3395A>C	ENSP00000480593.1:p.Asp1132Ala
ENST00000610817.5:c.3533A>C	ENSP00000480593.2:n.3533A>C
ENST00000673639.2:c.279+5117A>C
ENST00000676696.1:c.3755A>C	ENSP00000503392.1:n.3755A>C
XM_011531127.1:c.3476A>C	XP_011529429.1:p.Asp1159Ala
XM_011531128.1:c.3476A>C	XP_011529430.1:p.Asp1159Ala
XM_011531129.1:c.3476A>C	XP_011529431.1:p.Asp1159Ala
XM_011531130.1:c.3476A>C	XP_011529432.1:p.Asp1159Ala
XM_011531131.1:c.3275A>C	XP_011529433.1:p.Asp1092Ala