Canonical Allele Identifier: CA1229582076

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512098G= , CM000663.2:g.241512098G=	GRCh38
NC_000001.10:g.241675398G= , CM000663.1:g.241675398G=	GRCh37
NC_000001.9:g.239742021G=	NCBI36
NG_012338.1:g.12657C= , LRG_504:g.12657C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.927C=
ENST00000682162.1:c.453C=	ENSP00000508203.1:n.453C=
ENST00000682567.1:n.501C=
ENST00000683521.1:c.424C=	ENSP00000506864.1:p.Gln142=
ENST00000684483.1:c.424C=	ENSP00000507894.1:p.Gln142=
ENST00000366560.4:c.424C= MANE Select	ENSP00000355518.4:p.Gln142=
ENST00000366560.3:c.424C=	ENSP00000355518.3:p.Gln142=
ENST00000497042.1:n.120C=
NM_000143.3:c.424C= , LRG_504t1:c.424C=	NP_000134.2:p.Gln142=
XM_011544132.1:c.196C=	XP_011542434.1:p.Gln66=
XM_011544132.2:c.196C=	XP_011542434.1:p.Gln66=
NM_000143.4:c.424C= MANE Select	NP_000134.2:p.Gln142=