Canonical Allele Identifier: CA1229580719

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241508800T= , CM000663.2:g.241508800T=	GRCh38
NC_000001.10:g.241672100T= , CM000663.1:g.241672100T=	GRCh37
NC_000001.9:g.239738723T=	NCBI36
NG_012338.1:g.15955A= , LRG_504:g.15955A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1059-15A=
ENST00000682162.1:c.585-15A=	ENSP00000508203.1:n.585-15A=
ENST00000682567.1:n.633-15A=
ENST00000683521.1:c.556-15A=	ENSP00000506864.1:n.556-15A=
ENST00000684161.1:n.1756A=
ENST00000684483.1:c.556-40A=	ENSP00000507894.1:n.556-40A=
ENST00000366560.4:c.556-15A= MANE Select	ENSP00000355518.4:n.556-15A=
ENST00000366560.3:c.556-15A=	ENSP00000355518.3:n.556-15A=
NM_000143.3:c.556-15A= , LRG_504t1:c.556-15A=	NP_000134.2:n.556-15A=
XM_011544132.1:c.328-15A=	XP_011542434.1:n.328-15A=
XM_011544132.2:c.328-15A=	XP_011542434.1:n.328-15A=
NM_000143.4:c.556-15A= MANE Select	NP_000134.2:n.556-15A=