Canonical Allele Identifier: CA2542774368

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352755_154352765del , CM000685.2:g.154352755_154352765del	GRCh38
NC_000023.10:g.153581123_153581133del , CM000685.1:g.153581123_153581133del	GRCh37
NC_000023.9:g.153234317_153234327del	NCBI36
NG_011506.1:g.26874_26884del
NG_011506.2:g.26874_26884del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.6355+7_6355+17del	ENSP00000353467.4:n.6355+7_6355+17del
ENST00000369850.10:c.6379+7_6379+17del MANE Select	ENSP00000358866.3:n.6379+7_6379+17del
ENST00000369856.8:c.6298+7_6298+17del	ENSP00000358872.4:n.6298+7_6298+17del
ENST00000422373.6:c.3161-90_3161-80del	ENSP00000416926.2:n.3161-90_3161-80del
ENST00000610817.5:c.6436+7_6436+17del	ENSP00000480593.2:n.6436+7_6436+17del
ENST00000673639.2:c.280-4075_280-4065del
ENST00000676696.1:c.6658+7_6658+17del	ENSP00000503392.1:n.6658+7_6658+17del
ENST00000678304.1:n.1558+7_1558+17del
ENST00000344736.8:c.6259+7_6259+17del	ENSP00000358863.3:n.6259+7_6259+17del
ENST00000360319.8:c.6355+7_6355+17del	ENSP00000353467.4:n.6355+7_6355+17del
ENST00000369850.7:c.6379+7_6379+17del	ENSP00000358866.3:n.6379+7_6379+17del
ENST00000369856.7:c.6298+7_6298+17del	ENSP00000358872.4:n.6298+7_6298+17del
ENST00000415241.1:c.581+7_581+17del
ENST00000420627.5:c.6335+7_6335+17del	ENSP00000408921.1:n.6335+7_6335+17del
ENST00000422373.5:c.6355+7_6355+17del	ENSP00000416926.1:n.6355+7_6355+17del
ENST00000444578.1:c.322+7_322+17del	ENSP00000397824.1:n.322+7_322+17del
ENST00000466325.1:n.601_611del
ENST00000474358.5:n.12+7_12+17del
ENST00000490936.5:n.2368+7_2368+17del
ENST00000498411.1:n.67+52_67+62del
ENST00000610817.4:c.5844+628_5844+638del	ENSP00000480593.1:n.5844+628_5844+638del
NM_001110556.1:c.6379+7_6379+17del	NP_001104026.1:n.6379+7_6379+17del
NM_001456.3:c.6355+7_6355+17del	NP_001447.2:n.6355+7_6355+17del
XM_011531127.1:c.6283+7_6283+17del	XP_011529429.1:n.6283+7_6283+17del
XM_011531128.1:c.6259+7_6259+17del	XP_011529430.1:n.6259+7_6259+17del
XM_011531129.1:c.6205+7_6205+17del	XP_011529431.1:n.6205+7_6205+17del
XM_011531130.1:c.6181+7_6181+17del	XP_011529432.1:n.6181+7_6181+17del
XM_011531131.1:c.6178+7_6178+17del	XP_011529433.1:n.6178+7_6178+17del
NM_001110556.2:c.6379+7_6379+17del MANE Select	NP_001104026.1:n.6379+7_6379+17del
NM_001456.4:c.6355+7_6355+17del	NP_001447.2:n.6355+7_6355+17del