Canonical Allele Identifier: CA2824281312

Gene: FLNA

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154364721_154364821del , CM000685.2:g.154364721_154364821del	GRCh38
NC_000023.10:g.153593089_153593189del , CM000685.1:g.153593089_153593189del	GRCh37
NC_000023.9:g.153246283_153246383del	NCBI36
NG_011506.1:g.14820_14920del
NG_011506.2:g.14820_14920del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.1828+2_1829del
ENST00000369850.10:c.1828+2_1829del
ENST00000369856.8:c.1747+2_1748del
ENST00000422373.6:c.1828+2_1829del
ENST00000610817.5:c.1885+2_1886del
ENST00000673639.2:c.279+617_279+717del
ENST00000676696.1:c.2107+2_2108del
ENST00000344736.8:c.1828+2_1829del
ENST00000360319.8:c.1828+2_1829del
ENST00000369850.7:c.1828+2_1829del
ENST00000369856.7:c.1747+2_1748del
ENST00000420627.5:c.1784+2_1785del
ENST00000422373.5:c.1828+2_1829del
ENST00000465144.1:n.211_311del
ENST00000610817.4:c.1747+2_1748del
NM_001110556.1:c.1828+2_1829del
NM_001456.3:c.1828+2_1829del
XM_011531127.1:c.1828+2_1829del
XM_011531128.1:c.1828+2_1829del
XM_011531129.1:c.1828+2_1829del
XM_011531130.1:c.1828+2_1829del
XM_011531131.1:c.1627+2_1628del
NM_001110556.2:c.1828+2_1829del
NM_001456.4:c.1828+2_1829del