Canonical Allele Identifier: CA1143480628

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241506015C= , CM000663.2:g.241506015C=	GRCh38
NC_000001.10:g.241669315C= , CM000663.1:g.241669315C=	GRCh37
NC_000001.9:g.239735938C=	NCBI36
NG_012338.1:g.18740G= , LRG_504:g.18740G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1395G=
ENST00000682162.1:c.921G=	ENSP00000508203.1:n.921G=
ENST00000682567.1:n.969G=
ENST00000683521.1:c.892G=	ENSP00000506864.1:p.Ala298=
ENST00000684161.1:n.2107G=
ENST00000684483.1:c.*288G=	ENSP00000507894.1:n.*288G=
ENST00000366560.4:c.892G= MANE Select	ENSP00000355518.4:p.Ala298=
ENST00000366560.3:c.892G=	ENSP00000355518.3:p.Ala298=
NM_000143.3:c.892G= , LRG_504t1:c.892G=	NP_000134.2:p.Ala298=
XM_011544132.1:c.664G=	XP_011542434.1:p.Ala222=
XM_011544132.2:c.664G=	XP_011542434.1:p.Ala222=
NM_000143.4:c.892G= MANE Select	NP_000134.2:p.Ala298=