Canonical Allele Identifier: CA1138574780

Gene: FLNA

Linked Data

• dbSNP Id: rs2067678631
• gnomAD v3: X-154358382-TCAGA-T
• gnomAD v4: X-154358382-TCAGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154358386_154358389del , CM000685.2:g.154358386_154358389del	GRCh38
NC_000023.10:g.153586754_153586757del , CM000685.1:g.153586754_153586757del	GRCh37
NC_000023.9:g.153239948_153239951del	NCBI36
NG_011506.1:g.21253_21256del
NG_011506.2:g.21253_21256del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.4599-31_4599-28del	ENSP00000353467.4:n.4599-31_4599-28del
ENST00000369850.10:c.4599-31_4599-28del MANE Select	ENSP00000358866.3:n.4599-31_4599-28del
ENST00000369856.8:c.4518-31_4518-28del	ENSP00000358872.4:n.4518-31_4518-28del
ENST00000422373.6:c.3160+2969_3160+2972del	ENSP00000416926.2:n.3160+2969_3160+2972de...
ENST00000610817.5:c.4656-31_4656-28del	ENSP00000480593.2:n.4656-31_4656-28del
ENST00000673639.2:c.279+7050_279+7053del
ENST00000676696.1:c.4878-31_4878-28del	ENSP00000503392.1:n.4878-31_4878-28del
ENST00000678304.1:n.148+703_148+706del
ENST00000344736.8:c.4599-31_4599-28del	ENSP00000358863.3:n.4599-31_4599-28del
ENST00000360319.8:c.4599-31_4599-28del	ENSP00000353467.4:n.4599-31_4599-28del
ENST00000369850.7:c.4599-31_4599-28del	ENSP00000358866.3:n.4599-31_4599-28del
ENST00000369856.7:c.4518-31_4518-28del	ENSP00000358872.4:n.4518-31_4518-28del
ENST00000420627.5:c.4555-31_4555-28del	ENSP00000408921.1:n.4555-31_4555-28del
ENST00000422373.5:c.4599-31_4599-28del	ENSP00000416926.1:n.4599-31_4599-28del
ENST00000466319.1:n.221-31_221-28del
ENST00000490936.5:n.612-31_612-28del
ENST00000610817.4:c.4518-31_4518-28del	ENSP00000480593.1:n.4518-31_4518-28del
NM_001110556.1:c.4599-31_4599-28del	NP_001104026.1:n.4599-31_4599-28del
NM_001456.3:c.4599-31_4599-28del	NP_001447.2:n.4599-31_4599-28del
XM_011531127.1:c.4599-31_4599-28del	XP_011529429.1:n.4599-31_4599-28del
XM_011531128.1:c.4599-31_4599-28del	XP_011529430.1:n.4599-31_4599-28del
XM_011531129.1:c.4599-31_4599-28del	XP_011529431.1:n.4599-31_4599-28del
XM_011531130.1:c.4599-31_4599-28del	XP_011529432.1:n.4599-31_4599-28del
XM_011531131.1:c.4398-31_4398-28del	XP_011529433.1:n.4398-31_4398-28del
NM_001110556.2:c.4599-31_4599-28del MANE Select	NP_001104026.1:n.4599-31_4599-28del
NM_001456.4:c.4599-31_4599-28del	NP_001447.2:n.4599-31_4599-28del