Canonical Allele Identifier: CA873314729

Gene: FLNA

Linked Data

• dbSNP Id: rs1425793434
• MyVariant Identifiers: chrX:g.154371259A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154371259A>G , CM000685.2:g.154371259A>G	GRCh38
NC_000023.10:g.153599627A>G , CM000685.1:g.153599627A>G	GRCh37
NC_000023.9:g.153252821A>G	NCBI36
NG_008677.1:g.1832A>G , LRG_745:g.1832A>G
NG_011506.1:g.8380T>C
NG_011506.2:g.8380T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.-14T>C	ENSP00000353467.4:n.-14T>C
ENST00000369850.10:c.-14T>C MANE Select	ENSP00000358866.3:n.-14T>C
ENST00000422373.6:c.-14T>C	ENSP00000416926.2:n.-14T>C
ENST00000344736.8:c.-14T>C	ENSP00000358863.3:n.-14T>C
ENST00000360319.8:c.-14T>C	ENSP00000353467.4:n.-14T>C
ENST00000369850.7:c.-14T>C	ENSP00000358866.3:n.-14T>C
ENST00000422373.5:c.-14T>C	ENSP00000416926.1:n.-14T>C
ENST00000610817.4:c.-95T>C	ENSP00000480593.1:n.-95T>C
NM_001110556.1:c.-14T>C	NP_001104026.1:n.-14T>C
NM_001456.3:c.-14T>C	NP_001447.2:n.-14T>C
XM_011531127.1:c.-14T>C	XP_011529429.1:n.-14T>C
XM_011531128.1:c.-14T>C	XP_011529430.1:n.-14T>C
XM_011531129.1:c.-14T>C	XP_011529431.1:n.-14T>C
XM_011531130.1:c.-14T>C	XP_011529432.1:n.-14T>C
XM_011531131.1:c.-14T>C	XP_011529433.1:n.-14T>C
NM_001110556.2:c.-14T>C MANE Select	NP_001104026.1:n.-14T>C
NM_001456.4:c.-14T>C	NP_001447.2:n.-14T>C