Canonical Allele Identifier: CA1229580785

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508971T= , CM000663.2:g.241508971T=	GRCh38
NC_000001.10:g.241672271T= , CM000663.1:g.241672271T=	GRCh37
NC_000001.9:g.239738894T=	NCBI36
NG_012338.1:g.15784A= , LRG_504:g.15784A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1059-186A=
ENST00000682162.1:c.585-186A=	ENSP00000508203.1:n.585-186A=
ENST00000682567.1:n.633-186A=
ENST00000683521.1:c.556-186A=	ENSP00000506864.1:n.556-186A=
ENST00000684161.1:n.1585A=
ENST00000684483.1:c.556-211A=	ENSP00000507894.1:n.556-211A=
ENST00000366560.4:c.556-186A= MANE Select	ENSP00000355518.4:n.556-186A=
ENST00000366560.3:c.556-186A=	ENSP00000355518.3:n.556-186A=
NM_000143.3:c.556-186A= , LRG_504t1:c.556-186A=	NP_000134.2:n.556-186A=
XM_011544132.1:c.328-186A=	XP_011542434.1:n.328-186A=
XM_011544132.2:c.328-186A=	XP_011542434.1:n.328-186A=
NM_000143.4:c.556-186A= MANE Select	NP_000134.2:n.556-186A=