Canonical Allele Identifier: CA414608678

Gene: FHL1

Linked Data

• MyVariant Identifiers: chrX:g.135290121G>T (hg19) ; chrX:g.136207962G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136207962G>T , CM000685.2:g.136207962G>T	GRCh38
NC_000023.10:g.135290121G>T , CM000685.1:g.135290121G>T	GRCh37
NC_000023.9:g.135117787G>T	NCBI36
NG_015895.1:g.65563G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370683.6:c.549+1G>T MANE Select	ENSP00000359717.1:n.549+1G>T
ENST00000394155.8:c.501+1G>T MANE Plus Clinical	ENSP00000377710.2:n.501+1G>T
ENST00000628919.3:c.501+1G>T	ENSP00000487147.2:n.501+1G>T
ENST00000651089.1:c.501+1G>T	ENSP00000498684.1:n.501+1G>T
ENST00000651929.2:c.501+1G>T	ENSP00000499016.1:n.501+1G>T
ENST00000652457.1:c.501+1G>T	ENSP00000498503.1:n.501+1G>T
ENST00000345434.7:c.501+1G>T	ENSP00000071281.6:n.501+1G>T
ENST00000370674.3:c.501+1G>T	ENSP00000359708.1:n.501+1G>T
ENST00000370676.7:c.549+1G>T	ENSP00000359710.3:n.549+1G>T
ENST00000370683.5:c.549+1G>T	ENSP00000359717.1:n.549+1G>T
ENST00000370690.7:c.501+1G>T	ENSP00000359724.3:n.501+1G>T
ENST00000394153.6:c.501+1G>T	ENSP00000377709.2:n.501+1G>T
ENST00000394155.6:c.501+1G>T	ENSP00000377710.2:n.501+1G>T
ENST00000420362.5:c.501+1G>T	ENSP00000391779.1:n.501+1G>T
ENST00000434885.5:c.501+1G>T	ENSP00000413798.1:n.501+1G>T
ENST00000452016.5:c.501+1G>T	ENSP00000408038.1:n.501+1G>T
ENST00000456445.5:c.501+1G>T	ENSP00000412642.1:n.501+1G>T
ENST00000535737.5:c.501+1G>T	ENSP00000444815.1:n.501+1G>T
ENST00000539015.5:c.588+1G>T	ENSP00000437673.1:n.588+1G>T
ENST00000543669.5:c.501+1G>T	ENSP00000443333.1:n.501+1G>T
ENST00000618438.4:c.501+1G>T	ENSP00000477609.1:n.501+1G>T
ENST00000626004.1:n.205+1G>T
ENST00000628032.2:c.501+1G>T	ENSP00000487030.1:n.501+1G>T
ENST00000628568.1:c.501+1G>T	ENSP00000486782.1:n.501+1G>T
ENST00000629039.2:c.501+1G>T	ENSP00000486439.1:n.501+1G>T
ENST00000630084.2:c.501+1G>T	ENSP00000485897.1:n.501+1G>T
ENST00000630684.2:n.551+1G>T
NM_001159699.1:c.549+1G>T	NP_001153171.1:n.549+1G>T
NM_001159700.1:c.501+1G>T	NP_001153172.1:n.501+1G>T
NM_001159701.1:c.588+1G>T	NP_001153173.1:n.588+1G>T
NM_001159702.2:c.501+1G>T	NP_001153174.1:n.501+1G>T
NM_001159703.1:c.501+1G>T	NP_001153175.1:n.501+1G>T
NM_001159704.1:c.501+1G>T	NP_001153176.1:n.501+1G>T
NM_001167819.1:c.501+1G>T	NP_001161291.1:n.501+1G>T
NM_001449.4:c.501+1G>T	NP_001440.2:n.501+1G>T
NR_027621.1:n.912+1G>T
XM_006724743.2:c.549+1G>T	XP_006724806.1:n.549+1G>T
XM_006724744.2:c.501+1G>T	XP_006724807.1:n.501+1G>T
XM_006724745.2:c.501+1G>T	XP_006724808.1:n.501+1G>T
XM_006724746.2:c.501+1G>T	XP_006724809.1:n.501+1G>T
XM_006724747.2:c.501+1G>T	XP_006724810.1:n.501+1G>T
XM_011531316.1:c.549+1G>T	XP_011529618.1:n.549+1G>T
NM_001330659.1:c.549+1G>T	NP_001317588.1:n.549+1G>T
XM_006724744.3:c.501+1G>T	XP_006724807.1:n.501+1G>T
XM_006724745.4:c.501+1G>T	XP_006724808.1:n.501+1G>T
XM_006724746.3:c.501+1G>T	XP_006724809.1:n.501+1G>T
XM_006724747.3:c.501+1G>T	XP_006724810.1:n.501+1G>T
XM_017029357.2:c.501+1G>T	XP_016884846.1:n.501+1G>T
XM_024452353.1:c.501+1G>T	XP_024308121.1:n.501+1G>T
XM_024452354.1:c.501+1G>T	XP_024308122.1:n.501+1G>T
XM_024452355.1:c.501+1G>T	XP_024308123.1:n.501+1G>T
NM_001449.5:c.501+1G>T	NP_001440.2:n.501+1G>T
NM_001159699.2:c.549+1G>T MANE Select	NP_001153171.1:n.549+1G>T
NM_001159700.2:c.501+1G>T	NP_001153172.1:n.501+1G>T
NM_001159701.2:c.588+1G>T	NP_001153173.1:n.588+1G>T
NM_001159702.3:c.501+1G>T MANE Plus Clinical	NP_001153174.1:n.501+1G>T
NM_001159703.2:c.501+1G>T	NP_001153175.1:n.501+1G>T
NM_001330659.2:c.549+1G>T	NP_001317588.1:n.549+1G>T
NM_001369326.1:c.501+1G>T	NP_001356255.1:n.501+1G>T
NM_001369327.1:c.501+1G>T	NP_001356256.1:n.501+1G>T
NM_001369328.1:c.501+1G>T	NP_001356257.1:n.501+1G>T
NM_001369329.1:c.501+1G>T	NP_001356258.1:n.501+1G>T
NM_001369330.1:c.501+1G>T	NP_001356259.1:n.501+1G>T
NM_001369331.1:c.501+1G>T	NP_001356260.1:n.501+1G>T
NM_001369327.2:c.501+1G>T	NP_001356256.1:n.501+1G>T
NR_027621.2:n.912+1G>T