Canonical Allele Identifier: CA1229578831

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504173C= , CM000663.2:g.241504173C=	GRCh38
NC_000001.10:g.241667473C= , CM000663.1:g.241667473C=	GRCh37
NC_000001.9:g.239734096C=	NCBI36
NG_012338.1:g.20582G= , LRG_504:g.20582G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1480G=
ENST00000682162.1:c.1006G=	ENSP00000508203.1:n.1006G=
ENST00000682567.1:n.1054G=
ENST00000683521.1:c.977G=	ENSP00000506864.1:p.Gly326=
ENST00000684161.1:n.2192G=
ENST00000684483.1:c.*373G=	ENSP00000507894.1:n.*373G=
ENST00000366560.4:c.977G= MANE Select	ENSP00000355518.4:p.Gly326=
ENST00000366560.3:c.977G=	ENSP00000355518.3:p.Gly326=
NM_000143.3:c.977G= , LRG_504t1:c.977G=	NP_000134.2:p.Gly326=
XM_011544132.1:c.749G=	XP_011542434.1:p.Gly250=
XM_011544132.2:c.749G=	XP_011542434.1:p.Gly250=
NM_000143.4:c.977G= MANE Select	NP_000134.2:p.Gly326=