Canonical Allele Identifier: CA2694801096

Gene: FHL1

Linked Data

• gnomAD v4: X-136210298-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136210299del , CM000685.2:g.136210299del	GRCh38
NC_000023.10:g.135292458del , CM000685.1:g.135292458del	GRCh37
NC_000023.9:g.135120124del	NCBI36
NG_015895.1:g.67900del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370683.6:c.*274del MANE Select	ENSP00000359717.1:n.*274del
ENST00000394155.8:c.*345del MANE Plus Clinical	ENSP00000377710.2:n.*345del
ENST00000651089.1:c.*345del	ENSP00000498684.1:n.*345del
ENST00000651929.2:c.*274del	ENSP00000499016.1:n.*274del
ENST00000652457.1:c.*446del	ENSP00000498503.1:n.*446del
ENST00000345434.7:c.*345del	ENSP00000071281.6:n.*345del
ENST00000370683.5:c.*274del	ENSP00000359717.1:n.*274del
ENST00000370690.7:c.*274del	ENSP00000359724.3:n.*274del
ENST00000394153.6:c.*274del	ENSP00000377709.2:n.*274del
ENST00000394155.6:c.*345del	ENSP00000377710.2:n.*345del
ENST00000535737.5:c.*274del	ENSP00000444815.1:n.*274del
ENST00000539015.5:c.*274del	ENSP00000437673.1:n.*274del
ENST00000543669.5:c.*274del	ENSP00000443333.1:n.*274del
ENST00000618438.4:c.*345del	ENSP00000477609.1:n.*345del
ENST00000628568.1:c.*274del	ENSP00000486782.1:n.*274del
ENST00000630677.1:n.704del
NM_001159699.1:c.*274del	NP_001153171.1:n.*274del
NM_001159700.1:c.*274del	NP_001153172.1:n.*274del
NM_001159701.1:c.*274del	NP_001153173.1:n.*274del
NM_001159702.2:c.*345del	NP_001153174.1:n.*345del
NM_001159703.1:c.*345del	NP_001153175.1:n.*345del
NM_001159704.1:c.*274del	NP_001153176.1:n.*274del
NM_001167819.1:c.*274del	NP_001161291.1:n.*274del
NM_001449.4:c.*274del	NP_001440.2:n.*274del
NR_027621.1:n.1528del
XM_006724743.2:c.*345del	XP_006724806.1:n.*345del
XM_006724744.2:c.*345del	XP_006724807.1:n.*345del
XM_006724745.2:c.*345del	XP_006724808.1:n.*345del
XM_006724746.2:c.*345del	XP_006724809.1:n.*345del
XM_006724747.2:c.*274del	XP_006724810.1:n.*274del
XM_011531316.1:c.*345del	XP_011529618.1:n.*345del
NM_001330659.1:c.*345del	NP_001317588.1:n.*345del
XM_006724744.3:c.*345del	XP_006724807.1:n.*345del
XM_006724745.4:c.*345del	XP_006724808.1:n.*345del
XM_006724746.3:c.*345del	XP_006724809.1:n.*345del
XM_006724747.3:c.*274del	XP_006724810.1:n.*274del
XM_017029357.2:c.*274del	XP_016884846.1:n.*274del
XM_024452353.1:c.*345del	XP_024308121.1:n.*345del
XM_024452354.1:c.*345del	XP_024308122.1:n.*345del
XM_024452355.1:c.*274del	XP_024308123.1:n.*274del
NM_001449.5:c.*274del	NP_001440.2:n.*274del
NM_001159699.2:c.*274del MANE Select	NP_001153171.1:n.*274del
NM_001159700.2:c.*274del	NP_001153172.1:n.*274del
NM_001159701.2:c.*274del	NP_001153173.1:n.*274del
NM_001159702.3:c.*345del MANE Plus Clinical	NP_001153174.1:n.*345del
NM_001159703.2:c.*345del	NP_001153175.1:n.*345del
NM_001330659.2:c.*345del	NP_001317588.1:n.*345del
NM_001369326.1:c.*345del	NP_001356255.1:n.*345del
NM_001369327.1:c.*345del	NP_001356256.1:n.*345del
NM_001369328.1:c.*345del	NP_001356257.1:n.*345del
NM_001369329.1:c.*274del	NP_001356258.1:n.*274del
NM_001369330.1:c.*274del	NP_001356259.1:n.*274del
NM_001369331.1:c.*274del	NP_001356260.1:n.*274del
NM_001369327.2:c.*345del	NP_001356256.1:n.*345del
NR_027621.2:n.1528del