Canonical Allele Identifier: CA341137

Gene: FLNA

Linked Data

• ClinVar Variation Id: 11779
• ClinVar RCV Id: RCV000012546
• MyVariant Identifiers: chrX:g.153590180_153592124delinsCA (hg19) ; chrX:g.154361812_154363756delinsCA (hg38)
• PubMed: PMID:17190868 ; PMID:18223515 ; PMID:20301567 ; PMID:21773876

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154361812_154363756delinsCA , CM000685.2:g.154361812_154363756delinsCA	GRCh38
NC_000023.10:g.153590180_153592124delinsCA , CM000685.1:g.153590180_153592124delinsCA	GRCh37
NC_000023.9:g.153243374_153245318delinsCA	NCBI36
NG_011506.1:g.15883_17827delinsTG
NG_011506.2:g.15883_17827delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.2280+266_2827-25delinsTG
ENST00000369850.10:c.2280+266_2827-25delinsTG
ENST00000369856.8:c.2199+266_2746-25delinsTG
ENST00000422373.6:c.2280+266_2827-25delinsTG
ENST00000610817.5:c.2337+266_2884-25delinsTG
ENST00000673639.2:c.279+1680_279+3624delinsTG
ENST00000676696.1:c.2559+266_3106-25delinsTG
ENST00000344736.8:c.2280+266_2827-25delinsTG
ENST00000360319.8:c.2280+266_2827-25delinsTG
ENST00000369850.7:c.2280+266_2827-25delinsTG
ENST00000369856.7:c.2199+266_2746-25delinsTG
ENST00000420627.5:c.2236+266_2783-25delinsTG
ENST00000422373.5:c.2280+266_2827-25delinsTG
ENST00000610817.4:c.2199+266_2746-25delinsTG
NM_001110556.1:c.2280+266_2827-25delinsTG
NM_001456.3:c.2280+266_2827-25delinsTG
XM_011531127.1:c.2280+266_2827-25delinsTG
XM_011531128.1:c.2280+266_2827-25delinsTG
XM_011531129.1:c.2280+266_2827-25delinsTG
XM_011531130.1:c.2280+266_2827-25delinsTG
XM_011531131.1:c.2079+266_2626-25delinsTG
NM_001110556.2:c.2280+266_2827-25delinsTG
NM_001456.4:c.2280+266_2827-25delinsTG