Canonical Allele Identifier: CA10561483

Gene: FLNA

Linked Data

• ClinVar Variation Id: 392929
• ClinVar RCV Id: RCV000435884
• dbSNP Id: rs782455612
• ExAC: X:153599634 G / A
• gnomAD v2: X-153599634-G-A
• gnomAD v4: X-154371266-G-A
• MyVariant Identifiers: chrX:g.153599634G>A (hg19) ; chrX:g.154371266G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371266G>A , CM000685.2:g.154371266G>A	GRCh38
NC_000023.10:g.153599634G>A , CM000685.1:g.153599634G>A	GRCh37
NC_000023.9:g.153252828G>A	NCBI36
NG_008677.1:g.1839G>A , LRG_745:g.1839G>A
NG_011506.1:g.8373C>T
NG_011506.2:g.8373C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.-21C>T	ENSP00000353467.4:n.-21C>T
ENST00000369850.10:c.-21C>T MANE Select	ENSP00000358866.3:n.-21C>T
ENST00000422373.6:c.-21C>T	ENSP00000416926.2:n.-21C>T
ENST00000344736.8:c.-21C>T	ENSP00000358863.3:n.-21C>T
ENST00000360319.8:c.-21C>T	ENSP00000353467.4:n.-21C>T
ENST00000369850.7:c.-21C>T	ENSP00000358866.3:n.-21C>T
ENST00000422373.5:c.-21C>T	ENSP00000416926.1:n.-21C>T
ENST00000610817.4:c.-102C>T	ENSP00000480593.1:n.-102C>T
NM_001110556.1:c.-21C>T	NP_001104026.1:n.-21C>T
NM_001456.3:c.-21C>T	NP_001447.2:n.-21C>T
XM_011531127.1:c.-21C>T	XP_011529429.1:n.-21C>T
XM_011531128.1:c.-21C>T	XP_011529430.1:n.-21C>T
XM_011531129.1:c.-21C>T	XP_011529431.1:n.-21C>T
XM_011531130.1:c.-21C>T	XP_011529432.1:n.-21C>T
XM_011531131.1:c.-21C>T	XP_011529433.1:n.-21C>T
NM_001110556.2:c.-21C>T MANE Select	NP_001104026.1:n.-21C>T
NM_001456.4:c.-21C>T	NP_001447.2:n.-21C>T