Canonical Allele Identifier: CA1229578170

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241502561T= , CM000663.2:g.241502561T=	GRCh38
NC_000001.10:g.241665861T= , CM000663.1:g.241665861T=	GRCh37
NC_000001.9:g.239732484T=	NCBI36
NG_012338.1:g.22194A= , LRG_504:g.22194A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000143.4:c.1118A= MANE Select	NP_000134.2:p.Asn373=
ENST00000366560.4:c.1118A= MANE Select	ENSP00000355518.4:p.Asn373=
NM_000143.3:c.1118A= , LRG_504t1:c.1118A=	NP_000134.2:p.Asn373=
ENST00000366560.3:c.1118A=	ENSP00000355518.3:p.Asn373=
ENST00000493477.2:n.1621A=
ENST00000682162.1:c.1147A=	ENSP00000508203.1:n.1147A=
ENST00000682567.1:n.2666A=
ENST00000683521.1:c.1118A=	ENSP00000506864.1:p.Asn373=
ENST00000684161.1:n.2333A=
ENST00000684483.1:c.*514A=	ENSP00000507894.1:n.*514A=
XM_011544132.1:c.890A=	XP_011542434.1:p.Asn297=
XM_011544132.2:c.890A=	XP_011542434.1:p.Asn297=