Canonical Allele Identifier: CA424075658

Gene: FH

Linked Data

• MyVariant Identifiers: chr1:g.241665766A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502466A>G , CM000663.2:g.241502466A>G	GRCh38
NC_000001.10:g.241665766A>G , CM000663.1:g.241665766A>G	GRCh37
NC_000001.9:g.239732389A>G	NCBI36
NG_012338.1:g.22289T>C , LRG_504:g.22289T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1716T>C
ENST00000682162.1:c.1242T>C	ENSP00000508203.1:n.1242T>C
ENST00000682567.1:n.2761T>C
ENST00000683521.1:c.1213T>C	ENSP00000506864.1:p.Leu405=
ENST00000684161.1:n.2428T>C
ENST00000684483.1:c.*609T>C	ENSP00000507894.1:n.*609T>C
ENST00000366560.4:c.1213T>C MANE Select	ENSP00000355518.4:p.Leu405=
ENST00000366560.3:c.1213T>C	ENSP00000355518.3:p.Leu405=
NM_000143.3:c.1213T>C , LRG_504t1:c.1213T>C	NP_000134.2:p.Leu405=
XM_011544132.1:c.985T>C	XP_011542434.1:p.Leu329=
XM_011544132.2:c.985T>C	XP_011542434.1:p.Leu329=
NM_000143.4:c.1213T>C MANE Select	NP_000134.2:p.Leu405=