Canonical Allele Identifier: CA414609732

Gene: FHL1

Linked Data

• ClinVar Variation Id: 2797468
• ClinVar RCV Id: RCV003624785
• MyVariant Identifiers: chrX:g.135292085C>G (hg19) ; chrX:g.136209926C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136209926C>G , CM000685.2:g.136209926C>G	GRCh38
NC_000023.10:g.135292085C>G , CM000685.1:g.135292085C>G	GRCh37
NC_000023.9:g.135119751C>G	NCBI36
NG_015895.1:g.67527C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370683.6:c.792C>G MANE Select	ENSP00000359717.1:p.Tyr264Ter
ENST00000394155.8:c.944C>G MANE Plus Clinical	ENSP00000377710.2:p.Thr315Ser
ENST00000628919.3:c.744C>G	ENSP00000487147.2:p.Tyr248Ter
ENST00000651089.1:c.944C>G	ENSP00000498684.1:p.Thr315Ser
ENST00000651929.2:c.744C>G	ENSP00000499016.1:p.Tyr248Ter
ENST00000652457.1:c.*73C>G	ENSP00000498503.1:n.*73C>G
ENST00000345434.7:c.944C>G	ENSP00000071281.6:p.Thr315Ser
ENST00000370674.3:c.744C>G	ENSP00000359708.1:p.Tyr248Ter
ENST00000370676.7:c.605C>G	ENSP00000359710.3:p.Thr202Ser
ENST00000370683.5:c.792C>G	ENSP00000359717.1:p.Tyr264Ter
ENST00000370690.7:c.744C>G	ENSP00000359724.3:p.Tyr248Ter
ENST00000394153.6:c.744C>G	ENSP00000377709.2:p.Tyr248Ter
ENST00000394155.6:c.944C>G	ENSP00000377710.2:p.Thr315Ser
ENST00000535737.5:c.744C>G	ENSP00000444815.1:p.Tyr248Ter
ENST00000539015.5:c.831C>G	ENSP00000437673.1:p.Tyr277Ter
ENST00000543669.5:c.744C>G	ENSP00000443333.1:p.Tyr248Ter
ENST00000618438.4:c.557C>G	ENSP00000477609.1:p.Thr186Ser
ENST00000628568.1:c.744C>G	ENSP00000486782.1:p.Tyr248Ter
ENST00000629039.2:c.744C>G	ENSP00000486439.1:p.Tyr248Ter
ENST00000630084.2:c.744C>G	ENSP00000485897.1:p.Tyr248Ter
ENST00000630677.1:n.331C>G
NM_001159699.1:c.792C>G	NP_001153171.1:p.Tyr264Ter
NM_001159700.1:c.744C>G	NP_001153172.1:p.Tyr248Ter
NM_001159701.1:c.831C>G	NP_001153173.1:p.Tyr277Ter
NM_001159702.2:c.944C>G	NP_001153174.1:p.Thr315Ser
NM_001159703.1:c.557C>G	NP_001153175.1:p.Thr186Ser
NM_001159704.1:c.744C>G	NP_001153176.1:p.Tyr248Ter
NM_001167819.1:c.744C>G	NP_001161291.1:p.Tyr248Ter
NM_001449.4:c.744C>G	NP_001440.2:p.Tyr248Ter
NR_027621.1:n.1155C>G
XM_006724743.2:c.992C>G	XP_006724806.1:p.Thr331Ser
XM_006724744.2:c.944C>G	XP_006724807.1:p.Thr315Ser
XM_006724745.2:c.944C>G	XP_006724808.1:p.Thr315Ser
XM_006724746.2:c.944C>G	XP_006724809.1:p.Thr315Ser
XM_006724747.2:c.744C>G	XP_006724810.1:p.Tyr248Ter
XM_011531316.1:c.605C>G	XP_011529618.1:p.Thr202Ser
NM_001330659.1:c.605C>G	NP_001317588.1:p.Thr202Ser
XM_006724744.3:c.944C>G	XP_006724807.1:p.Thr315Ser
XM_006724745.4:c.944C>G	XP_006724808.1:p.Thr315Ser
XM_006724746.3:c.944C>G	XP_006724809.1:p.Thr315Ser
XM_006724747.3:c.744C>G	XP_006724810.1:p.Tyr248Ter
XM_017029357.2:c.744C>G	XP_016884846.1:p.Tyr248Ter
XM_024452353.1:c.944C>G	XP_024308121.1:p.Thr315Ser
XM_024452354.1:c.944C>G	XP_024308122.1:p.Thr315Ser
XM_024452355.1:c.744C>G	XP_024308123.1:p.Tyr248Ter
NM_001449.5:c.744C>G	NP_001440.2:p.Tyr248Ter
NM_001159699.2:c.792C>G MANE Select	NP_001153171.1:p.Tyr264Ter
NM_001159700.2:c.744C>G	NP_001153172.1:p.Tyr248Ter
NM_001159701.2:c.831C>G	NP_001153173.1:p.Tyr277Ter
NM_001159702.3:c.944C>G MANE Plus Clinical	NP_001153174.1:p.Thr315Ser
NM_001159703.2:c.557C>G	NP_001153175.1:p.Thr186Ser
NM_001330659.2:c.605C>G	NP_001317588.1:p.Thr202Ser
NM_001369326.1:c.944C>G	NP_001356255.1:p.Thr315Ser
NM_001369327.1:c.944C>G	NP_001356256.1:p.Thr315Ser
NM_001369328.1:c.944C>G	NP_001356257.1:p.Thr315Ser
NM_001369329.1:c.744C>G	NP_001356258.1:p.Tyr248Ter
NM_001369330.1:c.744C>G	NP_001356259.1:p.Tyr248Ter
NM_001369331.1:c.744C>G	NP_001356260.1:p.Tyr248Ter
NM_001369327.2:c.944C>G	NP_001356256.1:p.Thr315Ser
NR_027621.2:n.1155C>G