Canonical Allele Identifier: CA10561482

Gene: FLNA

Linked Data

• ClinVar Variation Id: 381207
• ClinVar RCV Id: RCV001703649 ; RCV003330668
• dbSNP Id: rs781821429
• ExAC: X:153599633 G / T
• gnomAD v2: X-153599633-G-T
• gnomAD v3: X-154371265-G-T
• gnomAD v4: X-154371265-G-T
• MyVariant Identifiers: chrX:g.153599633G>T (hg19) ; chrX:g.154371265G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371265G>T , CM000685.2:g.154371265G>T	GRCh38
NC_000023.10:g.153599633G>T , CM000685.1:g.153599633G>T	GRCh37
NC_000023.9:g.153252827G>T	NCBI36
NG_008677.1:g.1838G>T , LRG_745:g.1838G>T
NG_011506.1:g.8374C>A
NG_011506.2:g.8374C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.-20C>A	ENSP00000353467.4:n.-20C>A
ENST00000369850.10:c.-20C>A MANE Select	ENSP00000358866.3:n.-20C>A
ENST00000422373.6:c.-20C>A	ENSP00000416926.2:n.-20C>A
ENST00000344736.8:c.-20C>A	ENSP00000358863.3:n.-20C>A
ENST00000360319.8:c.-20C>A	ENSP00000353467.4:n.-20C>A
ENST00000369850.7:c.-20C>A	ENSP00000358866.3:n.-20C>A
ENST00000422373.5:c.-20C>A	ENSP00000416926.1:n.-20C>A
ENST00000610817.4:c.-101C>A	ENSP00000480593.1:n.-101C>A
NM_001110556.1:c.-20C>A	NP_001104026.1:n.-20C>A
NM_001456.3:c.-20C>A	NP_001447.2:n.-20C>A
XM_011531127.1:c.-20C>A	XP_011529429.1:n.-20C>A
XM_011531128.1:c.-20C>A	XP_011529430.1:n.-20C>A
XM_011531129.1:c.-20C>A	XP_011529431.1:n.-20C>A
XM_011531130.1:c.-20C>A	XP_011529432.1:n.-20C>A
XM_011531131.1:c.-20C>A	XP_011529433.1:n.-20C>A
NM_001110556.2:c.-20C>A MANE Select	NP_001104026.1:n.-20C>A
NM_001456.4:c.-20C>A	NP_001447.2:n.-20C>A