Canonical Allele Identifier: CA519706132

Gene: FLNA

Linked Data

• gnomAD v4: X-154352908-G-A
• MyVariant Identifiers: chrX:g.153581276G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154352908G>A , CM000685.2:g.154352908G>A	GRCh38
NC_000023.10:g.153581276G>A , CM000685.1:g.153581276G>A	GRCh37
NC_000023.9:g.153234470G>A	NCBI36
NG_011506.1:g.26731C>T
NG_011506.2:g.26731C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000360319.9:c.6219C>T	ENSP00000353467.4:p.Ser2073=
ENST00000369850.10:c.6243C>T MANE Select	ENSP00000358866.3:p.Ser2081=
ENST00000369856.8:c.6162C>T	ENSP00000358872.4:p.Ser2054=
ENST00000422373.6:c.3161-233C>T	ENSP00000416926.2:n.3161-233C>T
ENST00000610817.5:c.6300C>T	ENSP00000480593.2:n.6300C>T
ENST00000673639.2:c.280-4218C>T
ENST00000676696.1:c.6522C>T	ENSP00000503392.1:n.6522C>T
ENST00000678304.1:n.1422C>T
ENST00000344736.8:c.6123C>T	ENSP00000358863.3:p.Ser2041=
ENST00000360319.8:c.6219C>T	ENSP00000353467.4:p.Ser2073=
ENST00000369850.7:c.6243C>T	ENSP00000358866.3:p.Ser2081=
ENST00000369856.7:c.6162C>T	ENSP00000358872.4:p.Ser2054=
ENST00000415241.1:c.445C>T
ENST00000420627.5:c.6199C>T	ENSP00000408921.1:n.6199C>T
ENST00000422373.5:c.6219C>T	ENSP00000416926.1:p.Ser2073=
ENST00000444578.1:c.186C>T	ENSP00000397824.1:p.Ser62=
ENST00000466325.1:n.458C>T
ENST00000490936.5:n.2232C>T
ENST00000610817.4:c.5844+485C>T	ENSP00000480593.1:n.5844+485C>T
NM_001110556.1:c.6243C>T	NP_001104026.1:p.Ser2081=
NM_001456.3:c.6219C>T	NP_001447.2:p.Ser2073=
XM_011531127.1:c.6147C>T	XP_011529429.1:p.Ser2049=
XM_011531128.1:c.6123C>T	XP_011529430.1:p.Ser2041=
XM_011531129.1:c.6069C>T	XP_011529431.1:p.Ser2023=
XM_011531130.1:c.6045C>T	XP_011529432.1:p.Ser2015=
XM_011531131.1:c.6042C>T	XP_011529433.1:p.Ser2014=
NM_001110556.2:c.6243C>T MANE Select	NP_001104026.1:p.Ser2081=
NM_001456.4:c.6219C>T	NP_001447.2:p.Ser2073=