Canonical Allele Identifier: CA1141581482

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504066C= , CM000663.2:g.241504066C=	GRCh38
NC_000001.10:g.241667366C= , CM000663.1:g.241667366C=	GRCh37
NC_000001.9:g.239733989C=	NCBI36
NG_012338.1:g.20689G= , LRG_504:g.20689G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1587G=
ENST00000682162.1:c.1113G=	ENSP00000508203.1:n.1113G=
ENST00000682567.1:n.1161G=
ENST00000683521.1:c.1084G=	ENSP00000506864.1:p.Glu362=
ENST00000684161.1:n.2299G=
ENST00000684483.1:c.*480G=	ENSP00000507894.1:n.*480G=
ENST00000366560.4:c.1084G= MANE Select	ENSP00000355518.4:p.Glu362=
ENST00000366560.3:c.1084G=	ENSP00000355518.3:p.Glu362=
NM_000143.3:c.1084G= , LRG_504t1:c.1084G=	NP_000134.2:p.Glu362=
XM_011544132.1:c.856G=	XP_011542434.1:p.Glu286=
XM_011544132.2:c.856G=	XP_011542434.1:p.Glu286=
NM_000143.4:c.1084G= MANE Select	NP_000134.2:p.Glu362=