Canonical Allele Identifier: CA1229582028

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512002G= , CM000663.2:g.241512002G=	GRCh38
NC_000001.10:g.241675302G= , CM000663.1:g.241675302G=	GRCh37
NC_000001.9:g.239741925G=	NCBI36
NG_012338.1:g.12753C= , LRG_504:g.12753C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.1023C=
ENST00000682162.1:c.549C=	ENSP00000508203.1:n.549C=
ENST00000682567.1:n.597C=
ENST00000683521.1:c.520C=	ENSP00000506864.1:p.Pro174=
ENST00000684483.1:c.520C=	ENSP00000507894.1:p.Pro174=
ENST00000366560.4:c.520C= MANE Select	ENSP00000355518.4:p.Pro174=
ENST00000366560.3:c.520C=	ENSP00000355518.3:p.Pro174=
ENST00000497042.1:n.216C=
NM_000143.3:c.520C= , LRG_504t1:c.520C=	NP_000134.2:p.Pro174=
XM_011544132.1:c.292C=	XP_011542434.1:p.Pro98=
XM_011544132.2:c.292C=	XP_011542434.1:p.Pro98=
NM_000143.4:c.520C= MANE Select	NP_000134.2:p.Pro174=