Canonical Allele Identifier: CA274732

Gene: FLNA

Linked Data

• ClinVar Variation Id: 190191
• ClinVar RCV Id: RCV000170411
• dbSNP Id: rs786205190
• MyVariant Identifiers: chrX:g.153588004_153588019dup16 (hg19) ; chrX:g.153588003_153588004insGGAGTGCAGTCCTGGA (hg19) ; chrX:g.154359636_154359651dup16 (hg38) ; chrX:g.154359635_154359636insGGAGTGCAGTCCTGGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154359645_154359660dup , CM000685.2:g.154359645_154359660dup	GRCh38
NC_000023.10:g.153588013_153588028dup , CM000685.1:g.153588013_153588028dup	GRCh37
NC_000023.9:g.153241207_153241222dup	NCBI36
NG_011506.1:g.19988_20003dup
NG_011506.2:g.19988_20003dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.3980-5_3990dup
ENST00000369850.10:c.3980-5_3990dup
ENST00000369856.8:c.3899-5_3909dup
ENST00000422373.6:c.3160+1704_3160+1719dup	ENSP00000416926.2:n.3160+1704_3160+1719dup
ENST00000610817.5:c.4037-5_4047dup
ENST00000673639.2:c.279+5785_279+5800dup
ENST00000676696.1:c.4259-5_4269dup
ENST00000344736.8:c.3980-5_3990dup
ENST00000360319.8:c.3980-5_3990dup
ENST00000369850.7:c.3980-5_3990dup
ENST00000369856.7:c.3899-5_3909dup
ENST00000420627.5:c.3936-5_3946dup
ENST00000422373.5:c.3980-5_3990dup
ENST00000610817.4:c.3899-5_3909dup
NM_001110556.1:c.3980-5_3990dup
NM_001456.3:c.3980-5_3990dup
XM_011531127.1:c.3980-5_3990dup
XM_011531128.1:c.3980-5_3990dup
XM_011531129.1:c.3980-5_3990dup
XM_011531130.1:c.3980-5_3990dup
XM_011531131.1:c.3779-5_3789dup
NM_001110556.2:c.3980-5_3990dup
NM_001456.4:c.3980-5_3990dup