Canonical Allele Identifier: CA415237506

Gene: FLNA

Linked Data

• ClinVar Variation Id: 1328843
• ClinVar RCV Id: RCV001797475
• dbSNP Id: rs371839875
• MyVariant Identifiers: chrX:g.153591110A>C (hg19) ; chrX:g.154362742A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154362742A>C , CM000685.2:g.154362742A>C	GRCh38
NC_000023.10:g.153591110A>C , CM000685.1:g.153591110A>C	GRCh37
NC_000023.9:g.153244304A>C	NCBI36
NG_011506.1:g.16897T>G
NG_011506.2:g.16897T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360319.9:c.2323T>G	ENSP00000353467.4:p.Tyr775Asp
ENST00000369850.10:c.2323T>G MANE Select	ENSP00000358866.3:p.Tyr775Asp
ENST00000369856.8:c.2242T>G	ENSP00000358872.4:p.Tyr748Asp
ENST00000422373.6:c.2323T>G	ENSP00000416926.2:p.Tyr775Asp
ENST00000610817.5:c.2380T>G	ENSP00000480593.2:n.2380T>G
ENST00000673639.2:c.279+2694T>G
ENST00000676696.1:c.2602T>G	ENSP00000503392.1:n.2602T>G
ENST00000344736.8:c.2323T>G	ENSP00000358863.3:p.Tyr775Asp
ENST00000360319.8:c.2323T>G	ENSP00000353467.4:p.Tyr775Asp
ENST00000369850.7:c.2323T>G	ENSP00000358866.3:p.Tyr775Asp
ENST00000369856.7:c.2242T>G	ENSP00000358872.4:p.Tyr748Asp
ENST00000420627.5:c.2279T>G	ENSP00000408921.1:n.2279T>G
ENST00000422373.5:c.2323T>G	ENSP00000416926.1:p.Tyr775Asp
ENST00000610817.4:c.2242T>G	ENSP00000480593.1:p.Tyr748Asp
NM_001110556.1:c.2323T>G	NP_001104026.1:p.Tyr775Asp
NM_001456.3:c.2323T>G	NP_001447.2:p.Tyr775Asp
XM_011531127.1:c.2323T>G	XP_011529429.1:p.Tyr775Asp
XM_011531128.1:c.2323T>G	XP_011529430.1:p.Tyr775Asp
XM_011531129.1:c.2323T>G	XP_011529431.1:p.Tyr775Asp
XM_011531130.1:c.2323T>G	XP_011529432.1:p.Tyr775Asp
XM_011531131.1:c.2122T>G	XP_011529433.1:p.Tyr708Asp
NM_001110556.2:c.2323T>G MANE Select	NP_001104026.1:p.Tyr775Asp
NM_001456.4:c.2323T>G	NP_001447.2:p.Tyr775Asp