Canonical Allele Identifier: CA2466653284

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154353328_154353330delinsCAG , CM000685.2:g.154353328_154353330delinsCAG	GRCh38
NC_000023.10:g.153581696_153581698delinsCAG , CM000685.1:g.153581696_153581698delinsCAG	GRCh37
NC_000023.9:g.153234890_153234892delinsCAG	NCBI36
NG_011506.1:g.26309_26311delinsCTG
NG_011506.2:g.26309_26311delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.5964_5966delinsCTG	ENSP00000353467.4:p.Pro1988=
ENST00000369850.10:c.5988_5990delinsCTG MANE Select	ENSP00000358866.3:p.Pro1996=
ENST00000369856.8:c.5907_5909delinsCTG	ENSP00000358872.4:p.Pro1969=
ENST00000422373.6:c.3161-655_3161-653delinsCTG	ENSP00000416926.2:n.3161-655_3161-653delinsCTG
ENST00000610817.5:c.6045_6047delinsCTG	ENSP00000480593.2:n.6045_6047delinsCTG
ENST00000673639.2:c.280-4640_280-4638delinsCTG
ENST00000676696.1:c.6267_6269delinsCTG	ENSP00000503392.1:n.6267_6269delinsCTG
ENST00000678304.1:n.1167_1169delinsCTG
ENST00000344736.8:c.5868_5870delinsCTG	ENSP00000358863.3:p.Pro1956=
ENST00000360319.8:c.5964_5966delinsCTG	ENSP00000353467.4:p.Pro1988=
ENST00000369850.7:c.5988_5990delinsCTG	ENSP00000358866.3:p.Pro1996=
ENST00000369856.7:c.5907_5909delinsCTG	ENSP00000358872.4:p.Pro1969=
ENST00000415241.1:c.173_175delinsCTG
ENST00000420627.5:c.5944_5946delinsCTG	ENSP00000408921.1:n.5944_5946delinsCTG
ENST00000422373.5:c.5964_5966delinsCTG	ENSP00000416926.1:p.Pro1988=
ENST00000438732.2:c.662_664delinsCTG
ENST00000466325.1:n.127_129delinsCTG
ENST00000490936.5:n.1977_1979delinsCTG
ENST00000610817.4:c.5844+63_5844+65delinsCTG	ENSP00000480593.1:n.5844+63_5844+65delinsCTG
NM_001110556.1:c.5988_5990delinsCTG	NP_001104026.1:p.Pro1996=
NM_001456.3:c.5964_5966delinsCTG	NP_001447.2:p.Pro1988=
XM_011531127.1:c.5892_5894delinsCTG	XP_011529429.1:p.Pro1964=
XM_011531128.1:c.5868_5870delinsCTG	XP_011529430.1:p.Pro1956=
XM_011531129.1:c.5814_5816delinsCTG	XP_011529431.1:p.Pro1938=
XM_011531130.1:c.5790_5792delinsCTG	XP_011529432.1:p.Pro1930=
XM_011531131.1:c.5787_5789delinsCTG	XP_011529433.1:p.Pro1929=
NM_001110556.2:c.5988_5990delinsCTG MANE Select	NP_001104026.1:p.Pro1996=
NM_001456.4:c.5964_5966delinsCTG	NP_001447.2:p.Pro1988=