Canonical Allele Identifier: CA2460260318
Gene: FHL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136210032_136210041delinsAGGGGCTCCT , CM000685.2:g.136210032_136210041delinsAGGGGCTCCT GRCh38
NC_000023.10:g.135292191_135292200delinsAGGGGCTCCT , CM000685.1:g.135292191_135292200delinsAGGGGCTCCT GRCh37
NC_000023.9:g.135119857_135119866delinsAGGGGCTCCT NCBI36
NG_015895.1:g.67633_67642delinsAGGGGCTCCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370683.6:c.*7_*16delinsAGGGGCTCCT MANE Select ENSP00000359717.1:n.*7_*16delinsAGGGGCTCCT
ENST00000394155.8:c.*78_*87delinsAGGGGCTCCT MANE Plus Clinical ENSP00000377710.2:n.*78_*87delinsAGGGGCTCCT
ENST00000628919.3:c.*7_*16delinsAGGGGCTCCT ENSP00000487147.2:n.*7_*16delinsAGGGGCTCCT
ENST00000651089.1:c.*78_*87delinsAGGGGCTCCT ENSP00000498684.1:n.*78_*87delinsAGGGGCTCCT
ENST00000651929.2:c.*7_*16delinsAGGGGCTCCT ENSP00000499016.1:n.*7_*16delinsAGGGGCTCCT
ENST00000652457.1:c.*179_*188delinsAGGGGCTCCT ENSP00000498503.1:n.*179_*188delinsAGGGGCTCCT
ENST00000345434.7:c.*78_*87delinsAGGGGCTCCT ENSP00000071281.6:n.*78_*87delinsAGGGGCTCCT
ENST00000370676.7:c.*78_*87delinsAGGGGCTCCT ENSP00000359710.3:n.*78_*87delinsAGGGGCTCCT
ENST00000370683.5:c.*7_*16delinsAGGGGCTCCT ENSP00000359717.1:n.*7_*16delinsAGGGGCTCCT
ENST00000370690.7:c.*7_*16delinsAGGGGCTCCT ENSP00000359724.3:n.*7_*16delinsAGGGGCTCCT
ENST00000394153.6:c.*7_*16delinsAGGGGCTCCT ENSP00000377709.2:n.*7_*16delinsAGGGGCTCCT
ENST00000394155.6:c.*78_*87delinsAGGGGCTCCT ENSP00000377710.2:n.*78_*87delinsAGGGGCTCCT
ENST00000535737.5:c.*7_*16delinsAGGGGCTCCT ENSP00000444815.1:n.*7_*16delinsAGGGGCTCCT
ENST00000539015.5:c.*7_*16delinsAGGGGCTCCT ENSP00000437673.1:n.*7_*16delinsAGGGGCTCCT
ENST00000543669.5:c.*7_*16delinsAGGGGCTCCT ENSP00000443333.1:n.*7_*16delinsAGGGGCTCCT
ENST00000618438.4:c.*78_*87delinsAGGGGCTCCT ENSP00000477609.1:n.*78_*87delinsAGGGGCTCCT
ENST00000628568.1:c.*7_*16delinsAGGGGCTCCT ENSP00000486782.1:n.*7_*16delinsAGGGGCTCCT
ENST00000629039.2:c.*7_*16delinsAGGGGCTCCT ENSP00000486439.1:n.*7_*16delinsAGGGGCTCCT
ENST00000630084.2:c.*7_*16delinsAGGGGCTCCT ENSP00000485897.1:n.*7_*16delinsAGGGGCTCCT
ENST00000630677.1:n.437_446delinsAGGGGCTCCT
NM_001159699.1:c.*7_*16delinsAGGGGCTCCT NP_001153171.1:n.*7_*16delinsAGGGGCTCCT
NM_001159700.1:c.*7_*16delinsAGGGGCTCCT NP_001153172.1:n.*7_*16delinsAGGGGCTCCT
NM_001159701.1:c.*7_*16delinsAGGGGCTCCT NP_001153173.1:n.*7_*16delinsAGGGGCTCCT
NM_001159702.2:c.*78_*87delinsAGGGGCTCCT NP_001153174.1:n.*78_*87delinsAGGGGCTCCT
NM_001159703.1:c.*78_*87delinsAGGGGCTCCT NP_001153175.1:n.*78_*87delinsAGGGGCTCCT
NM_001159704.1:c.*7_*16delinsAGGGGCTCCT NP_001153176.1:n.*7_*16delinsAGGGGCTCCT
NM_001167819.1:c.*7_*16delinsAGGGGCTCCT NP_001161291.1:n.*7_*16delinsAGGGGCTCCT
NM_001449.4:c.*7_*16delinsAGGGGCTCCT NP_001440.2:n.*7_*16delinsAGGGGCTCCT
NR_027621.1:n.1261_1270delinsAGGGGCTCCT
XM_006724743.2:c.*78_*87delinsAGGGGCTCCT XP_006724806.1:n.*78_*87delinsAGGGGCTCCT
XM_006724744.2:c.*78_*87delinsAGGGGCTCCT XP_006724807.1:n.*78_*87delinsAGGGGCTCCT
XM_006724745.2:c.*78_*87delinsAGGGGCTCCT XP_006724808.1:n.*78_*87delinsAGGGGCTCCT
XM_006724746.2:c.*78_*87delinsAGGGGCTCCT XP_006724809.1:n.*78_*87delinsAGGGGCTCCT
XM_006724747.2:c.*7_*16delinsAGGGGCTCCT XP_006724810.1:n.*7_*16delinsAGGGGCTCCT
XM_011531316.1:c.*78_*87delinsAGGGGCTCCT XP_011529618.1:n.*78_*87delinsAGGGGCTCCT
NM_001330659.1:c.*78_*87delinsAGGGGCTCCT NP_001317588.1:n.*78_*87delinsAGGGGCTCCT
XM_006724744.3:c.*78_*87delinsAGGGGCTCCT XP_006724807.1:n.*78_*87delinsAGGGGCTCCT
XM_006724745.4:c.*78_*87delinsAGGGGCTCCT XP_006724808.1:n.*78_*87delinsAGGGGCTCCT
XM_006724746.3:c.*78_*87delinsAGGGGCTCCT XP_006724809.1:n.*78_*87delinsAGGGGCTCCT
XM_006724747.3:c.*7_*16delinsAGGGGCTCCT XP_006724810.1:n.*7_*16delinsAGGGGCTCCT
XM_017029357.2:c.*7_*16delinsAGGGGCTCCT XP_016884846.1:n.*7_*16delinsAGGGGCTCCT
XM_024452353.1:c.*78_*87delinsAGGGGCTCCT XP_024308121.1:n.*78_*87delinsAGGGGCTCCT
XM_024452354.1:c.*78_*87delinsAGGGGCTCCT XP_024308122.1:n.*78_*87delinsAGGGGCTCCT
XM_024452355.1:c.*7_*16delinsAGGGGCTCCT XP_024308123.1:n.*7_*16delinsAGGGGCTCCT
NM_001449.5:c.*7_*16delinsAGGGGCTCCT NP_001440.2:n.*7_*16delinsAGGGGCTCCT
NM_001159699.2:c.*7_*16delinsAGGGGCTCCT MANE Select NP_001153171.1:n.*7_*16delinsAGGGGCTCCT
NM_001159700.2:c.*7_*16delinsAGGGGCTCCT NP_001153172.1:n.*7_*16delinsAGGGGCTCCT
NM_001159701.2:c.*7_*16delinsAGGGGCTCCT NP_001153173.1:n.*7_*16delinsAGGGGCTCCT
NM_001159702.3:c.*78_*87delinsAGGGGCTCCT MANE Plus Clinical NP_001153174.1:n.*78_*87delinsAGGGGCTCCT
NM_001159703.2:c.*78_*87delinsAGGGGCTCCT NP_001153175.1:n.*78_*87delinsAGGGGCTCCT
NM_001330659.2:c.*78_*87delinsAGGGGCTCCT NP_001317588.1:n.*78_*87delinsAGGGGCTCCT
NM_001369326.1:c.*78_*87delinsAGGGGCTCCT NP_001356255.1:n.*78_*87delinsAGGGGCTCCT
NM_001369327.1:c.*78_*87delinsAGGGGCTCCT NP_001356256.1:n.*78_*87delinsAGGGGCTCCT
NM_001369328.1:c.*78_*87delinsAGGGGCTCCT NP_001356257.1:n.*78_*87delinsAGGGGCTCCT
NM_001369329.1:c.*7_*16delinsAGGGGCTCCT NP_001356258.1:n.*7_*16delinsAGGGGCTCCT
NM_001369330.1:c.*7_*16delinsAGGGGCTCCT NP_001356259.1:n.*7_*16delinsAGGGGCTCCT
NM_001369331.1:c.*7_*16delinsAGGGGCTCCT NP_001356260.1:n.*7_*16delinsAGGGGCTCCT
NM_001369327.2:c.*78_*87delinsAGGGGCTCCT NP_001356256.1:n.*78_*87delinsAGGGGCTCCT
NR_027621.2:n.1261_1270delinsAGGGGCTCCT