Canonical Allele Identifier: CA1229580636

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508649A= , CM000663.2:g.241508649A=	GRCh38
NC_000001.10:g.241671949A= , CM000663.1:g.241671949A=	GRCh37
NC_000001.9:g.239738572A=	NCBI36
NG_012338.1:g.16106T= , LRG_504:g.16106T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1195T=
ENST00000682162.1:c.721T=	ENSP00000508203.1:n.721T=
ENST00000682567.1:n.769T=
ENST00000683521.1:c.692T=	ENSP00000506864.1:p.Ile231=
ENST00000684161.1:n.1907T=
ENST00000684483.1:c.*88T=	ENSP00000507894.1:n.*88T=
ENST00000366560.4:c.692T= MANE Select	ENSP00000355518.4:p.Ile231=
ENST00000366560.3:c.692T=	ENSP00000355518.3:p.Ile231=
NM_000143.3:c.692T= , LRG_504t1:c.692T=	NP_000134.2:p.Ile231=
XM_011544132.1:c.464T=	XP_011542434.1:p.Ile155=
XM_011544132.2:c.464T=	XP_011542434.1:p.Ile155=
NM_000143.4:c.692T= MANE Select	NP_000134.2:p.Ile231=