Canonical Allele Identifier: CA1140925905

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241513679C= , CM000663.2:g.241513679C=	GRCh38
NC_000001.10:g.241676979C= , CM000663.1:g.241676979C=	GRCh37
NC_000001.9:g.239743602C=	NCBI36
NG_012338.1:g.11076G= , LRG_504:g.11076G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.805G=
ENST00000682162.1:c.331G=	ENSP00000508203.1:n.331G=
ENST00000682567.1:n.379G=
ENST00000683521.1:c.302G=	ENSP00000506864.1:p.Arg101=
ENST00000684483.1:c.302G=	ENSP00000507894.1:p.Arg101=
ENST00000366560.4:c.302G= MANE Select	ENSP00000355518.4:p.Arg101=
ENST00000366560.3:c.302G=	ENSP00000355518.3:p.Arg101=
NM_000143.3:c.302G= , LRG_504t1:c.302G=	NP_000134.2:p.Arg101=
XM_011544132.1:c.74G=	XP_011542434.1:p.Arg25=
XM_011544132.2:c.74G=	XP_011542434.1:p.Arg25=
NM_000143.4:c.302G= MANE Select	NP_000134.2:p.Arg101=