Canonical Allele Identifier: CA1229580791

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508995T= , CM000663.2:g.241508995T=	GRCh38
NC_000001.10:g.241672295T= , CM000663.1:g.241672295T=	GRCh37
NC_000001.9:g.239738918T=	NCBI36
NG_012338.1:g.15760A= , LRG_504:g.15760A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1059-210A=
ENST00000682162.1:c.585-210A=	ENSP00000508203.1:n.585-210A=
ENST00000682567.1:n.633-210A=
ENST00000683521.1:c.556-210A=	ENSP00000506864.1:n.556-210A=
ENST00000684161.1:n.1561A=
ENST00000684483.1:c.556-235A=	ENSP00000507894.1:n.556-235A=
ENST00000366560.4:c.556-210A= MANE Select	ENSP00000355518.4:n.556-210A=
ENST00000366560.3:c.556-210A=	ENSP00000355518.3:n.556-210A=
NM_000143.3:c.556-210A= , LRG_504t1:c.556-210A=	NP_000134.2:n.556-210A=
XM_011544132.1:c.328-210A=	XP_011542434.1:n.328-210A=
XM_011544132.2:c.328-210A=	XP_011542434.1:n.328-210A=
NM_000143.4:c.556-210A= MANE Select	NP_000134.2:n.556-210A=