Canonical Allele Identifier: CA1229582119

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512196T= , CM000663.2:g.241512196T=	GRCh38
NC_000001.10:g.241675496T= , CM000663.1:g.241675496T=	GRCh37
NC_000001.9:g.239742119T=	NCBI36
NG_012338.1:g.12559A= , LRG_504:g.12559A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.882-53A=
ENST00000682162.1:c.408-53A=	ENSP00000508203.1:n.408-53A=
ENST00000682567.1:n.456-53A=
ENST00000683521.1:c.379-53A=	ENSP00000506864.1:n.379-53A=
ENST00000684483.1:c.379-53A=	ENSP00000507894.1:n.379-53A=
ENST00000366560.4:c.379-53A= MANE Select	ENSP00000355518.4:n.379-53A=
ENST00000366560.3:c.379-53A=	ENSP00000355518.3:n.379-53A=
ENST00000497042.1:n.75-53A=
NM_000143.3:c.379-53A= , LRG_504t1:c.379-53A=	NP_000134.2:n.379-53A=
XM_011544132.1:c.151-53A=	XP_011542434.1:n.151-53A=
XM_011544132.2:c.151-53A=	XP_011542434.1:n.151-53A=
NM_000143.4:c.379-53A= MANE Select	NP_000134.2:n.379-53A=