Canonical Allele Identifier: CA10525129
Gene: FHL1 HGNC NCBI

Linked Data

ClinVar Variation Id: 569001
dbSNP Id: rs190006104

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136209951G>A , CM000685.2:g.136209951G>A GRCh38
NC_000023.10:g.135292110G>A , CM000685.1:g.135292110G>A GRCh37
NC_000023.9:g.135119776G>A NCBI36
NG_015895.1:g.67552G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000370683.6:c.817G>A MANE Select ENSP00000359717.1:p.Val273Met
ENST00000394155.8:c.969G>A MANE Plus Clinical ENSP00000377710.2:p.Pro323=
ENST00000628919.3:c.769G>A ENSP00000487147.2:p.Val257Met
ENST00000651089.1:c.969G>A ENSP00000498684.1:p.Pro323=
ENST00000651929.2:c.769G>A ENSP00000499016.1:p.Val257Met
ENST00000652457.1:c.*98G>A ENSP00000498503.1:n.*98G>A
ENST00000345434.7:c.969G>A ENSP00000071281.6:p.Pro323=
ENST00000370674.3:c.769G>A ENSP00000359708.1:p.Val257Met
ENST00000370676.7:c.630G>A ENSP00000359710.3:p.Pro210=
ENST00000370683.5:c.817G>A ENSP00000359717.1:p.Val273Met
ENST00000370690.7:c.769G>A ENSP00000359724.3:p.Val257Met
ENST00000394153.6:c.769G>A ENSP00000377709.2:p.Val257Met
ENST00000394155.6:c.969G>A ENSP00000377710.2:p.Pro323=
ENST00000535737.5:c.769G>A ENSP00000444815.1:p.Val257Met
ENST00000539015.5:c.856G>A ENSP00000437673.1:p.Val286Met
ENST00000543669.5:c.769G>A ENSP00000443333.1:p.Val257Met
ENST00000618438.4:c.582G>A ENSP00000477609.1:p.Pro194=
ENST00000628568.1:c.769G>A ENSP00000486782.1:p.Val257Met
ENST00000629039.2:c.769G>A ENSP00000486439.1:p.Val257Met
ENST00000630084.2:c.769G>A ENSP00000485897.1:p.Val257Met
ENST00000630677.1:n.356G>A
NM_001159699.1:c.817G>A NP_001153171.1:p.Val273Met
NM_001159700.1:c.769G>A NP_001153172.1:p.Val257Met
NM_001159701.1:c.856G>A NP_001153173.1:p.Val286Met
NM_001159702.2:c.969G>A NP_001153174.1:p.Pro323=
NM_001159703.1:c.582G>A NP_001153175.1:p.Pro194=
NM_001159704.1:c.769G>A NP_001153176.1:p.Val257Met
NM_001167819.1:c.769G>A NP_001161291.1:p.Val257Met
NM_001449.4:c.769G>A NP_001440.2:p.Val257Met
NR_027621.1:n.1180G>A
XM_006724743.2:c.1017G>A XP_006724806.1:p.Pro339=
XM_006724744.2:c.969G>A XP_006724807.1:p.Pro323=
XM_006724745.2:c.969G>A XP_006724808.1:p.Pro323=
XM_006724746.2:c.969G>A XP_006724809.1:p.Pro323=
XM_006724747.2:c.769G>A XP_006724810.1:p.Val257Met
XM_011531316.1:c.630G>A XP_011529618.1:p.Pro210=
NM_001330659.1:c.630G>A NP_001317588.1:p.Pro210=
XM_006724744.3:c.969G>A XP_006724807.1:p.Pro323=
XM_006724745.4:c.969G>A XP_006724808.1:p.Pro323=
XM_006724746.3:c.969G>A XP_006724809.1:p.Pro323=
XM_006724747.3:c.769G>A XP_006724810.1:p.Val257Met
XM_017029357.2:c.769G>A XP_016884846.1:p.Val257Met
XM_024452353.1:c.969G>A XP_024308121.1:p.Pro323=
XM_024452354.1:c.969G>A XP_024308122.1:p.Pro323=
XM_024452355.1:c.769G>A XP_024308123.1:p.Val257Met
NM_001449.5:c.769G>A NP_001440.2:p.Val257Met
NM_001159699.2:c.817G>A MANE Select NP_001153171.1:p.Val273Met
NM_001159700.2:c.769G>A NP_001153172.1:p.Val257Met
NM_001159701.2:c.856G>A NP_001153173.1:p.Val286Met
NM_001159702.3:c.969G>A MANE Plus Clinical NP_001153174.1:p.Pro323=
NM_001159703.2:c.582G>A NP_001153175.1:p.Pro194=
NM_001330659.2:c.630G>A NP_001317588.1:p.Pro210=
NM_001369326.1:c.969G>A NP_001356255.1:p.Pro323=
NM_001369327.1:c.969G>A NP_001356256.1:p.Pro323=
NM_001369328.1:c.969G>A NP_001356257.1:p.Pro323=
NM_001369329.1:c.769G>A NP_001356258.1:p.Val257Met
NM_001369330.1:c.769G>A NP_001356259.1:p.Val257Met
NM_001369331.1:c.769G>A NP_001356260.1:p.Val257Met
NM_001369327.2:c.969G>A NP_001356256.1:p.Pro323=
NR_027621.2:n.1180G>A