Canonical Allele Identifier: CA10525110

Gene: FHL1

Linked Data

• dbSNP Id: rs766836412
• ExAC: X:135292017 T / TTTTC
• gnomAD v2: X-135292017-T-TTTTC
• gnomAD v3: X-136209858-T-TTTTC
• gnomAD v4: X-136209858-T-TTTTC
• MyVariant Identifiers: chrX:g.135292021_135292022delinsCTTTTC (hg19) ; chrX:g.135292017_135292018insTTTC (hg19) ; chrX:g.136209858_136209859insTTTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136209861_136209862insCTTT , CM000685.2:g.136209861_136209862insCTTT	GRCh38
NC_000023.10:g.135292020_135292021insCTTT , CM000685.1:g.135292020_135292021insCTTT	GRCh37
NC_000023.9:g.135119686_135119687insCTTT	NCBI36
NG_015895.1:g.67462_67463insCTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000370683.6:c.737-10_737-9insCTTT MANE Select	ENSP00000359717.1:n.737-10_737-9insCTTT
ENST00000394155.8:c.889-10_889-9insCTTT MANE Plus Clinical	ENSP00000377710.2:n.889-10_889-9insCTTT
ENST00000628919.3:c.689-10_689-9insCTTT	ENSP00000487147.2:n.689-10_689-9insCTTT
ENST00000651089.1:c.889-10_889-9insCTTT	ENSP00000498684.1:n.889-10_889-9insCTTT
ENST00000651929.2:c.689-10_689-9insCTTT	ENSP00000499016.1:n.689-10_689-9insCTTT
ENST00000652457.1:c.*18-10_*18-9insCTTT	ENSP00000498503.1:n.*18-10_*18-9insCTTT
ENST00000345434.7:c.889-10_889-9insCTTT	ENSP00000071281.6:n.889-10_889-9insCTTT
ENST00000370674.3:c.689-10_689-9insCTTT	ENSP00000359708.1:n.689-10_689-9insCTTT
ENST00000370676.7:c.550-10_550-9insCTTT	ENSP00000359710.3:n.550-10_550-9insCTTT
ENST00000370683.5:c.737-10_737-9insCTTT	ENSP00000359717.1:n.737-10_737-9insCTTT
ENST00000370690.7:c.689-10_689-9insCTTT	ENSP00000359724.3:n.689-10_689-9insCTTT
ENST00000394153.6:c.689-10_689-9insCTTT	ENSP00000377709.2:n.689-10_689-9insCTTT
ENST00000394155.6:c.889-10_889-9insCTTT	ENSP00000377710.2:n.889-10_889-9insCTTT
ENST00000535737.5:c.689-10_689-9insCTTT	ENSP00000444815.1:n.689-10_689-9insCTTT
ENST00000539015.5:c.776-10_776-9insCTTT	ENSP00000437673.1:n.776-10_776-9insCTTT
ENST00000543669.5:c.689-10_689-9insCTTT	ENSP00000443333.1:n.689-10_689-9insCTTT
ENST00000618438.4:c.502-10_502-9insCTTT	ENSP00000477609.1:n.502-10_502-9insCTTT
ENST00000628568.1:c.689-10_689-9insCTTT	ENSP00000486782.1:n.689-10_689-9insCTTT
ENST00000629039.2:c.689-10_689-9insCTTT	ENSP00000486439.1:n.689-10_689-9insCTTT
ENST00000630084.2:c.689-10_689-9insCTTT	ENSP00000485897.1:n.689-10_689-9insCTTT
ENST00000630677.1:n.276-10_276-9insCTTT
NM_001159699.1:c.737-10_737-9insCTTT	NP_001153171.1:n.737-10_737-9insCTTT
NM_001159700.1:c.689-10_689-9insCTTT	NP_001153172.1:n.689-10_689-9insCTTT
NM_001159701.1:c.776-10_776-9insCTTT	NP_001153173.1:n.776-10_776-9insCTTT
NM_001159702.2:c.889-10_889-9insCTTT	NP_001153174.1:n.889-10_889-9insCTTT
NM_001159703.1:c.502-10_502-9insCTTT	NP_001153175.1:n.502-10_502-9insCTTT
NM_001159704.1:c.689-10_689-9insCTTT	NP_001153176.1:n.689-10_689-9insCTTT
NM_001167819.1:c.689-10_689-9insCTTT	NP_001161291.1:n.689-10_689-9insCTTT
NM_001449.4:c.689-10_689-9insCTTT	NP_001440.2:n.689-10_689-9insCTTT
NR_027621.1:n.1100-10_1100-9insCTTT
XM_006724743.2:c.937-10_937-9insCTTT	XP_006724806.1:n.937-10_937-9insCTTT
XM_006724744.2:c.889-10_889-9insCTTT	XP_006724807.1:n.889-10_889-9insCTTT
XM_006724745.2:c.889-10_889-9insCTTT	XP_006724808.1:n.889-10_889-9insCTTT
XM_006724746.2:c.889-10_889-9insCTTT	XP_006724809.1:n.889-10_889-9insCTTT
XM_006724747.2:c.689-10_689-9insCTTT	XP_006724810.1:n.689-10_689-9insCTTT
XM_011531316.1:c.550-10_550-9insCTTT	XP_011529618.1:n.550-10_550-9insCTTT
NM_001330659.1:c.550-10_550-9insCTTT	NP_001317588.1:n.550-10_550-9insCTTT
XM_006724744.3:c.889-10_889-9insCTTT	XP_006724807.1:n.889-10_889-9insCTTT
XM_006724745.4:c.889-10_889-9insCTTT	XP_006724808.1:n.889-10_889-9insCTTT
XM_006724746.3:c.889-10_889-9insCTTT	XP_006724809.1:n.889-10_889-9insCTTT
XM_006724747.3:c.689-10_689-9insCTTT	XP_006724810.1:n.689-10_689-9insCTTT
XM_017029357.2:c.689-10_689-9insCTTT	XP_016884846.1:n.689-10_689-9insCTTT
XM_024452353.1:c.889-10_889-9insCTTT	XP_024308121.1:n.889-10_889-9insCTTT
XM_024452354.1:c.889-10_889-9insCTTT	XP_024308122.1:n.889-10_889-9insCTTT
XM_024452355.1:c.689-10_689-9insCTTT	XP_024308123.1:n.689-10_689-9insCTTT
NM_001449.5:c.689-10_689-9insCTTT	NP_001440.2:n.689-10_689-9insCTTT
NM_001159699.2:c.737-10_737-9insCTTT MANE Select	NP_001153171.1:n.737-10_737-9insCTTT
NM_001159700.2:c.689-10_689-9insCTTT	NP_001153172.1:n.689-10_689-9insCTTT
NM_001159701.2:c.776-10_776-9insCTTT	NP_001153173.1:n.776-10_776-9insCTTT
NM_001159702.3:c.889-10_889-9insCTTT MANE Plus Clinical	NP_001153174.1:n.889-10_889-9insCTTT
NM_001159703.2:c.502-10_502-9insCTTT	NP_001153175.1:n.502-10_502-9insCTTT
NM_001330659.2:c.550-10_550-9insCTTT	NP_001317588.1:n.550-10_550-9insCTTT
NM_001369326.1:c.889-10_889-9insCTTT	NP_001356255.1:n.889-10_889-9insCTTT
NM_001369327.1:c.889-10_889-9insCTTT	NP_001356256.1:n.889-10_889-9insCTTT
NM_001369328.1:c.889-10_889-9insCTTT	NP_001356257.1:n.889-10_889-9insCTTT
NM_001369329.1:c.689-10_689-9insCTTT	NP_001356258.1:n.689-10_689-9insCTTT
NM_001369330.1:c.689-10_689-9insCTTT	NP_001356259.1:n.689-10_689-9insCTTT
NM_001369331.1:c.689-10_689-9insCTTT	NP_001356260.1:n.689-10_689-9insCTTT
NM_001369327.2:c.889-10_889-9insCTTT	NP_001356256.1:n.889-10_889-9insCTTT
NR_027621.2:n.1100-10_1100-9insCTTT