Canonical Allele Identifier: CA1229582069

Gene: FH

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.241512090T= , CM000663.2:g.241512090T=	GRCh38
NC_000001.10:g.241675390T= , CM000663.1:g.241675390T=	GRCh37
NC_000001.9:g.239742013T=	NCBI36
NG_012338.1:g.12665A= , LRG_504:g.12665A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000493477.2:n.935A=
ENST00000682162.1:c.461A=	ENSP00000508203.1:n.461A=
ENST00000682567.1:n.509A=
ENST00000683521.1:c.432A=	ENSP00000506864.1:p.Gly144=
ENST00000684483.1:c.432A=	ENSP00000507894.1:p.Gly144=
ENST00000366560.4:c.432A= MANE Select	ENSP00000355518.4:p.Gly144=
ENST00000366560.3:c.432A=	ENSP00000355518.3:p.Gly144=
ENST00000497042.1:n.128A=
NM_000143.3:c.432A= , LRG_504t1:c.432A=	NP_000134.2:p.Gly144=
XM_011544132.1:c.204A=	XP_011542434.1:p.Gly68=
XM_011544132.2:c.204A=	XP_011542434.1:p.Gly68=
NM_000143.4:c.432A= MANE Select	NP_000134.2:p.Gly144=