Canonical Allele Identifier: CA1229584148

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241517326A= , CM000663.2:g.241517326A=	GRCh38
NC_000001.10:g.241680626A= , CM000663.1:g.241680626A=	GRCh37
NC_000001.9:g.239747249A=	NCBI36
NG_012338.1:g.7429T= , LRG_504:g.7429T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.636-10T=
ENST00000682162.1:c.162-10T=	ENSP00000508203.1:n.162-10T=
ENST00000682567.1:n.210-10T=
ENST00000683521.1:c.133-10T=	ENSP00000506864.1:n.133-10T=
ENST00000684483.1:c.133-10T=	ENSP00000507894.1:n.133-10T=
ENST00000366560.4:c.133-10T= MANE Select	ENSP00000355518.4:n.133-10T=
ENST00000366560.3:c.133-10T=	ENSP00000355518.3:n.133-10T=
ENST00000493477.1:n.246-10T=
NM_000143.3:c.133-10T= , LRG_504t1:c.133-10T=	NP_000134.2:n.133-10T=
XM_011544132.1:c.-96-10T=	XP_011542434.1:n.-96-10T=
XM_011544132.2:c.-96-10T=	XP_011542434.1:n.-96-10T=
NM_000143.4:c.133-10T= MANE Select	NP_000134.2:n.133-10T=