Canonical Allele Identifier: CA1146108612

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512440G= , CM000663.2:g.241512440G=	GRCh38
NC_000001.10:g.241675740G= , CM000663.1:g.241675740G=	GRCh37
NC_000001.9:g.239742363G=	NCBI36
NG_012338.1:g.12315C= , LRG_504:g.12315C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.882-297C=
ENST00000682162.1:c.408-297C=	ENSP00000508203.1:n.408-297C=
ENST00000682567.1:n.456-297C=
ENST00000683521.1:c.379-297C=	ENSP00000506864.1:n.379-297C=
ENST00000684483.1:c.379-297C=	ENSP00000507894.1:n.379-297C=
ENST00000366560.4:c.379-297C= MANE Select	ENSP00000355518.4:n.379-297C=
ENST00000366560.3:c.379-297C=	ENSP00000355518.3:n.379-297C=
ENST00000497042.1:n.75-297C=
NM_000143.3:c.379-297C= , LRG_504t1:c.379-297C=	NP_000134.2:n.379-297C=
XM_011544132.1:c.151-297C=	XP_011542434.1:n.151-297C=
XM_011544132.2:c.151-297C=	XP_011542434.1:n.151-297C=
NM_000143.4:c.379-297C= MANE Select	NP_000134.2:n.379-297C=