Canonical Allele Identifier: CA323849
Gene: FLNA HGNC NCBI

Linked Data

dbSNP Id: rs863223628
MyVariant Identifiers: chrX:g.153596323T>G (hg19) chrX:g.154367955T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154367955T>G , CM000685.2:g.154367955T>G GRCh38
NC_000023.10:g.153596323T>G , CM000685.1:g.153596323T>G GRCh37
NC_000023.9:g.153249517T>G NCBI36
NG_011506.1:g.11684A>C
NG_011506.2:g.11684A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360319.9:c.509A>C ENSP00000353467.4:p.Gln170Pro
ENST00000369850.10:c.509A>C MANE Select ENSP00000358866.3:p.Gln170Pro
ENST00000369856.8:c.428A>C ENSP00000358872.4:p.Gln143Pro
ENST00000422373.6:c.509A>C ENSP00000416926.2:p.Gln170Pro
ENST00000610817.5:c.509A>C ENSP00000480593.2:p.Gln170Pro
ENST00000676696.1:c.509A>C ENSP00000503392.1:p.Gln170Pro
ENST00000344736.8:c.509A>C ENSP00000358863.3:p.Gln170Pro
ENST00000360319.8:c.509A>C ENSP00000353467.4:p.Gln170Pro
ENST00000369850.7:c.509A>C ENSP00000358866.3:p.Gln170Pro
ENST00000369856.7:c.428A>C ENSP00000358872.4:p.Gln143Pro
ENST00000420627.5:c.467A>C ENSP00000408921.1:p.Gln156Pro
ENST00000422373.5:c.509A>C ENSP00000416926.1:p.Gln170Pro
ENST00000610817.4:c.428A>C ENSP00000480593.1:p.Gln143Pro
NM_001110556.1:c.509A>C NP_001104026.1:p.Gln170Pro
NM_001456.3:c.509A>C NP_001447.2:p.Gln170Pro
XM_011531127.1:c.509A>C XP_011529429.1:p.Gln170Pro
XM_011531128.1:c.509A>C XP_011529430.1:p.Gln170Pro
XM_011531129.1:c.509A>C XP_011529431.1:p.Gln170Pro
XM_011531130.1:c.509A>C XP_011529432.1:p.Gln170Pro
XM_011531131.1:c.509A>C XP_011529433.1:p.Gln170Pro
NM_001110556.2:c.509A>C MANE Select NP_001104026.1:p.Gln170Pro
NM_001456.4:c.509A>C NP_001447.2:p.Gln170Pro
Search 100 bp 5'
Search 100 bp 3'