Canonical Allele Identifier: CA2543120571

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352718_154352719insCGGCA , CM000685.2:g.154352718_154352719insCGGCA	GRCh38
NC_000023.10:g.153581086_153581087insCGGCA , CM000685.1:g.153581086_153581087insCGGCA	GRCh37
NC_000023.9:g.153234280_153234281insCGGCA	NCBI36
NG_011506.1:g.26920_26921insTGCCG
NG_011506.2:g.26920_26921insTGCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6356-44_6356-43insTGCCG	ENSP00000353467.4:n.6356-44_6356-43insTGCCG
ENST00000369850.10:c.6380-44_6380-43insTGCCG MANE Select	ENSP00000358866.3:n.6380-44_6380-43insTGCCG
ENST00000369856.8:c.6299-44_6299-43insTGCCG	ENSP00000358872.4:n.6299-44_6299-43insTGCCG
ENST00000422373.6:c.3161-44_3161-43insTGCCG	ENSP00000416926.2:n.3161-44_3161-43insTGCCG
ENST00000610817.5:c.6437-44_6437-43insTGCCG	ENSP00000480593.2:n.6437-44_6437-43insTGCCG
ENST00000673639.2:c.280-4029_280-4028insTGCCG
ENST00000676696.1:c.6659-44_6659-43insTGCCG	ENSP00000503392.1:n.6659-44_6659-43insTGCCG
ENST00000678304.1:n.1559-44_1559-43insTGCCG
ENST00000344736.8:c.6260-44_6260-43insTGCCG	ENSP00000358863.3:n.6260-44_6260-43insTGCCG
ENST00000360319.8:c.6356-44_6356-43insTGCCG	ENSP00000353467.4:n.6356-44_6356-43insTGCCG
ENST00000369850.7:c.6380-44_6380-43insTGCCG	ENSP00000358866.3:n.6380-44_6380-43insTGCCG
ENST00000369856.7:c.6299-44_6299-43insTGCCG	ENSP00000358872.4:n.6299-44_6299-43insTGCCG
ENST00000415241.1:c.582-44_582-43insTGCCG
ENST00000420627.5:c.6336-44_6336-43insTGCCG	ENSP00000408921.1:n.6336-44_6336-43insTGCCG
ENST00000422373.5:c.6356-44_6356-43insTGCCG	ENSP00000416926.1:n.6356-44_6356-43insTGCCG
ENST00000444578.1:c.322+53_322+54insTGCCG	ENSP00000397824.1:n.322+53_322+54insTGCCG
ENST00000466325.1:n.647_648insTGCCG
ENST00000474358.5:n.13-44_13-43insTGCCG
ENST00000490936.5:n.2369-44_2369-43insTGCCG
ENST00000498411.1:n.67+98_67+99insTGCCG
ENST00000610817.4:c.5844+674_5844+675insTGCCG	ENSP00000480593.1:n.5844+674_5844+675insTGCCG
NM_001110556.1:c.6380-44_6380-43insTGCCG	NP_001104026.1:n.6380-44_6380-43insTGCCG
NM_001456.3:c.6356-44_6356-43insTGCCG	NP_001447.2:n.6356-44_6356-43insTGCCG
XM_011531127.1:c.6284-44_6284-43insTGCCG	XP_011529429.1:n.6284-44_6284-43insTGCCG
XM_011531128.1:c.6260-44_6260-43insTGCCG	XP_011529430.1:n.6260-44_6260-43insTGCCG
XM_011531129.1:c.6206-44_6206-43insTGCCG	XP_011529431.1:n.6206-44_6206-43insTGCCG
XM_011531130.1:c.6182-44_6182-43insTGCCG	XP_011529432.1:n.6182-44_6182-43insTGCCG
XM_011531131.1:c.6179-44_6179-43insTGCCG	XP_011529433.1:n.6179-44_6179-43insTGCCG
NM_001110556.2:c.6380-44_6380-43insTGCCG MANE Select	NP_001104026.1:n.6380-44_6380-43insTGCCG
NM_001456.4:c.6356-44_6356-43insTGCCG	NP_001447.2:n.6356-44_6356-43insTGCCG