Canonical Allele Identifier: CA1229578899

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241504332T= , CM000663.2:g.241504332T=	GRCh38
NC_000001.10:g.241667632T= , CM000663.1:g.241667632T=	GRCh37
NC_000001.9:g.239734255T=	NCBI36
NG_012338.1:g.20423A= , LRG_504:g.20423A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1408-87A=
ENST00000682162.1:c.934-87A=	ENSP00000508203.1:n.934-87A=
ENST00000682567.1:n.982-87A=
ENST00000683521.1:c.905-87A=	ENSP00000506864.1:n.905-87A=
ENST00000684161.1:n.2120-87A=
ENST00000684483.1:c.*301-87A=	ENSP00000507894.1:n.*301-87A=
ENST00000366560.4:c.905-87A= MANE Select	ENSP00000355518.4:n.905-87A=
ENST00000366560.3:c.905-87A=	ENSP00000355518.3:n.905-87A=
NM_000143.3:c.905-87A= , LRG_504t1:c.905-87A=	NP_000134.2:n.905-87A=
XM_011544132.1:c.677-87A=	XP_011542434.1:n.677-87A=
XM_011544132.2:c.677-87A=	XP_011542434.1:n.677-87A=
NM_000143.4:c.905-87A= MANE Select	NP_000134.2:n.905-87A=