Canonical Allele Identifier: CA1229582016

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241511968T= , CM000663.2:g.241511968T=	GRCh38
NC_000001.10:g.241675268T= , CM000663.1:g.241675268T=	GRCh37
NC_000001.9:g.239741891T=	NCBI36
NG_012338.1:g.12787A= , LRG_504:g.12787A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1057A=
ENST00000682162.1:c.583A=	ENSP00000508203.1:n.583A=
ENST00000682567.1:n.631A=
ENST00000683521.1:c.554A=	ENSP00000506864.1:p.Gln185=
ENST00000684483.1:c.554A=	ENSP00000507894.1:p.Gln185=
ENST00000366560.4:c.554A= MANE Select	ENSP00000355518.4:p.Gln185=
ENST00000366560.3:c.554A=	ENSP00000355518.3:p.Gln185=
ENST00000497042.1:n.250A=
NM_000143.3:c.554A= , LRG_504t1:c.554A=	NP_000134.2:p.Gln185=
XM_011544132.1:c.326A=	XP_011542434.1:p.Gln109=
XM_011544132.2:c.326A=	XP_011542434.1:p.Gln109=
NM_000143.4:c.554A= MANE Select	NP_000134.2:p.Gln185=